EP3454844A4 - COMBINATION THERAPIES OF HDAC INHIBITORS AND PD-1 INHIBITORS - Google Patents
COMBINATION THERAPIES OF HDAC INHIBITORS AND PD-1 INHIBITORS Download PDFInfo
- Publication number
- EP3454844A4 EP3454844A4 EP17796865.8A EP17796865A EP3454844A4 EP 3454844 A4 EP3454844 A4 EP 3454844A4 EP 17796865 A EP17796865 A EP 17796865A EP 3454844 A4 EP3454844 A4 EP 3454844A4
- Authority
- EP
- European Patent Office
- Prior art keywords
- inhibitors
- combination therapies
- hdac
- hdac inhibitors
- therapies
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000012270 PD-1 inhibitor Substances 0.000 title 1
- 239000012668 PD-1-inhibitor Substances 0.000 title 1
- 238000002648 combination therapy Methods 0.000 title 1
- 239000003276 histone deacetylase inhibitor Substances 0.000 title 1
- 229940121655 pd-1 inhibitor Drugs 0.000 title 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2803—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
- C07K16/2818—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against CD28 or CD152
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/18—Sulfonamides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4406—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/15—Depsipeptides; Derivatives thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/39541—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against normal tissues, cells
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/39558—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against tumor tissues, cells, antigens
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2803—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
- C07K16/2827—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against B7 molecules, e.g. CD80, CD86
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/545—Medicinal preparations containing antigens or antibodies characterised by the dose, timing or administration schedule
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Biomedical Technology (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Gastroenterology & Hepatology (AREA)
- Pain & Pain Management (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP24185599.8A EP4450085A3 (en) | 2016-05-11 | 2017-05-11 | Treatment of colon cancer with a combination of the hdac inhibitor hbi-800 and a pd-l1 inhibitor |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201662335044P | 2016-05-11 | 2016-05-11 | |
US201662436361P | 2016-12-19 | 2016-12-19 | |
PCT/US2017/032218 WO2017197153A1 (en) | 2016-05-11 | 2017-05-11 | Combination therapies of hdac inhibitors pd-1 inhibitors |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP24185599.8A Division EP4450085A3 (en) | 2016-05-11 | 2017-05-11 | Treatment of colon cancer with a combination of the hdac inhibitor hbi-800 and a pd-l1 inhibitor |
Publications (3)
Publication Number | Publication Date |
---|---|
EP3454844A1 EP3454844A1 (en) | 2019-03-20 |
EP3454844A4 true EP3454844A4 (en) | 2020-01-15 |
EP3454844B1 EP3454844B1 (en) | 2024-07-03 |
Family
ID=60267478
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP17796865.8A Active EP3454844B1 (en) | 2016-05-11 | 2017-05-11 | Treatment of colon cancer with a combination of the hdac inhibitor hbi-8000 and a pd-l1 inhibitor |
EP24185599.8A Pending EP4450085A3 (en) | 2016-05-11 | 2017-05-11 | Treatment of colon cancer with a combination of the hdac inhibitor hbi-800 and a pd-l1 inhibitor |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP24185599.8A Pending EP4450085A3 (en) | 2016-05-11 | 2017-05-11 | Treatment of colon cancer with a combination of the hdac inhibitor hbi-800 and a pd-l1 inhibitor |
Country Status (16)
Country | Link |
---|---|
US (4) | US10385130B2 (en) |
EP (2) | EP3454844B1 (en) |
JP (2) | JP7013387B2 (en) |
KR (2) | KR102469268B1 (en) |
CN (1) | CN109562177A (en) |
AU (2) | AU2017263478B2 (en) |
BR (1) | BR112018073329A2 (en) |
CA (1) | CA3023549A1 (en) |
DK (1) | DK3454844T3 (en) |
ES (1) | ES2988149T3 (en) |
IL (1) | IL262814B2 (en) |
MA (1) | MA44991A (en) |
MX (2) | MX2018013591A (en) |
PT (1) | PT3454844T (en) |
TW (1) | TWI808055B (en) |
WO (1) | WO2017197153A1 (en) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2905525T3 (en) | 2015-05-06 | 2022-04-11 | Snipr Tech Ltd | Alteration of microbial populations and modification of the microbiota |
TWI808055B (en) | 2016-05-11 | 2023-07-11 | 美商滬亞生物國際有限公司 | Combination therapies of hdac inhibitors and pd-1 inhibitors |
TWI794171B (en) | 2016-05-11 | 2023-03-01 | 美商滬亞生物國際有限公司 | Combination therapies of hdac inhibitors and pd-l1 inhibitors |
GB201609811D0 (en) | 2016-06-05 | 2016-07-20 | Snipr Technologies Ltd | Methods, cells, systems, arrays, RNA and kits |
JP7187486B2 (en) | 2017-05-25 | 2022-12-12 | レイドス, インコーポレイテッド | PD-1 and CTLA-4 Dual Inhibitor Peptides |
JOP20200024A1 (en) | 2017-08-04 | 2020-02-02 | Bayer Ag | Dihydrooxadiazinones |
EP3661917B1 (en) | 2017-08-04 | 2022-05-11 | Bayer Aktiengesellschaft | 6-((3-trifluoromethyl)phenyl)-4,5-dihydropyridazin-3(2h)-one derivatives as pde3a and pde3b inhibitors for treating cancer |
AU2019200033B2 (en) * | 2018-01-05 | 2020-09-10 | Gnt Biotech & Medicals Corporation | A pharmaceutical combination and method for regulation of tumor microenvironment and immunotherapy |
US12128018B2 (en) | 2018-01-12 | 2024-10-29 | KDAc Therapeutics, Inc. | Combination of a selective histone deacetylase 3 (HDAC3) inhibitor and an immunotherapy agent for the treatment of cancer |
JP7170737B2 (en) | 2018-02-27 | 2022-11-14 | レイドス, インコーポレイテッド | PD-1 peptide inhibitor |
US10760075B2 (en) | 2018-04-30 | 2020-09-01 | Snipr Biome Aps | Treating and preventing microbial infections |
US11851663B2 (en) | 2018-10-14 | 2023-12-26 | Snipr Biome Aps | Single-vector type I vectors |
CN111195249B (en) * | 2018-11-20 | 2023-11-28 | 深圳微芯生物科技股份有限公司 | Application of Sidamide combined with R-CHOP and combined medicine |
CN109912686B (en) * | 2019-03-13 | 2022-07-05 | 北京大学深圳研究生院 | Stable polypeptide inhibitor targeting HDAC (Histone deacetylase) and application thereof |
CA3141162A1 (en) | 2019-05-22 | 2020-11-26 | Leidos, Inc. | Lag3 binding peptides |
WO2020247830A1 (en) * | 2019-06-06 | 2020-12-10 | Huya Bioscience International, Llc | Triplet therapies of hdac inhibitors, pd-l1 and/or pd-1 inhibitors, and ctla-4 inhibitors |
WO2021037128A1 (en) * | 2019-08-28 | 2021-03-04 | 深圳微芯生物科技股份有限公司 | Chidamide-containing pharmaceutical composition and use thereof |
KR20210028339A (en) | 2019-09-04 | 2021-03-12 | 크리스탈지노믹스(주) | Pharmaceutical composition using hdac inhibitor and anti pd-1 antibody or anti pd-l1 antibody |
US11878009B2 (en) * | 2019-09-10 | 2024-01-23 | Great Novel Therapeutics Biotech & Medicals Corporation | Anticancer combination of chidamide and celecoxib salts |
CA3153597A1 (en) | 2019-09-11 | 2021-03-18 | Gnt Biotech & Medicals Corporation | An anticancer combination of chidamide and celecoxib |
TW202128224A (en) * | 2019-12-23 | 2021-08-01 | 大陸商信達生物製藥(蘇州)有限公司 | Pharmaceutical combination of anti-pd-1 antibody and histone deacetylase inhibitor, use and application method thereof |
CN111190006A (en) * | 2020-03-09 | 2020-05-22 | 上海市东方医院(同济大学附属东方医院) | Use of histone deacetylase 6 in the preparation of a marker for assessing peritoneal function in maintenance peritoneal dialysis patients |
JP2023529839A (en) | 2020-06-04 | 2023-07-12 | レイドス, インコーポレイテッド | immunomodulatory compounds |
EP4188947A2 (en) | 2020-07-31 | 2023-06-07 | Leidos, Inc. | Lag3 binding peptides |
US20220110924A1 (en) * | 2020-08-25 | 2022-04-14 | Huyabio International, Llc | Methods and compositions for genetic modulation of tumor microenvironments |
WO2022081426A1 (en) | 2020-10-12 | 2022-04-21 | Leidos, Inc. | Immunomodulatory peptides |
GB202209518D0 (en) | 2022-06-29 | 2022-08-10 | Snipr Biome Aps | Treating & preventing E coli infections |
KR20240043709A (en) * | 2022-09-27 | 2024-04-03 | 사회복지법인 삼성생명공익재단 | Composition for treating cancer comprising histone deacetylase inhibitor, and anticancer adjuvant for cancer immunotherapy |
WO2024231293A1 (en) * | 2023-05-05 | 2024-11-14 | Euro-Celtique S.A. | Combinations for treating cancer |
CN117924505B (en) * | 2024-03-25 | 2024-09-13 | 青岛宝迈得生物科技有限公司 | Recombinant HDAC2 protein monoclonal antibody and application thereof |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015157162A1 (en) * | 2014-04-06 | 2015-10-15 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Histone deacetylase as a modulator of pdl1 expression and activity |
Family Cites Families (538)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH627446A5 (en) | 1978-01-17 | 1982-01-15 | Debiopharm Sa | NEW BENZAMIDE DERIVATIVES. |
GB8302483D0 (en) | 1983-01-29 | 1983-03-02 | Beecham Group Plc | Compounds |
US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
US6548640B1 (en) | 1986-03-27 | 2003-04-15 | Btg International Limited | Altered antibodies |
CZ284687B6 (en) | 1986-04-30 | 1999-02-17 | Dainippon Pharmaceutical Co., Ltd. | Substituted benzamide derivative, process of its preparation and pharmaceutical composition based thereon |
GB8823869D0 (en) | 1988-10-12 | 1988-11-16 | Medical Res Council | Production of antibodies |
US6075181A (en) | 1990-01-12 | 2000-06-13 | Abgenix, Inc. | Human antibodies derived from immunized xenomice |
ATE356869T1 (en) | 1990-01-12 | 2007-04-15 | Amgen Fremont Inc | FORMATION OF XENOGENE ANTIBODIES |
US6150584A (en) | 1990-01-12 | 2000-11-21 | Abgenix, Inc. | Human antibodies derived from immunized xenomice |
US5545806A (en) | 1990-08-29 | 1996-08-13 | Genpharm International, Inc. | Ransgenic non-human animals for producing heterologous antibodies |
US5661016A (en) | 1990-08-29 | 1997-08-26 | Genpharm International Inc. | Transgenic non-human animals capable of producing heterologous antibodies of various isotypes |
US5633425A (en) | 1990-08-29 | 1997-05-27 | Genpharm International, Inc. | Transgenic non-human animals capable of producing heterologous antibodies |
US5625126A (en) | 1990-08-29 | 1997-04-29 | Genpharm International, Inc. | Transgenic non-human animals for producing heterologous antibodies |
DE69127627T2 (en) | 1990-08-29 | 1998-02-19 | Genpharm Int | Production and Use Non-human transgene heterologous antibodies for production |
JP2529912B2 (en) | 1990-10-16 | 1996-09-04 | 帝国化学産業株式会社 | Benzamide derivative |
US5395832A (en) | 1991-02-15 | 1995-03-07 | Hokuriku Seiyaku Co., Ltd. | Benzamide derivatives |
TW219935B (en) | 1991-12-25 | 1994-02-01 | Mitsubishi Chemicals Co Ltd | |
US5236931A (en) | 1992-03-26 | 1993-08-17 | A. H. Robins Company, Incorporated | 2-substituted benzamide and benzoate derivatives of 3-aminoquinuclidine and 3-quinuclidinol |
US5610052A (en) | 1992-08-26 | 1997-03-11 | Ribozyme Pharmaceuticals Inc. | Enzymatic RNA with activity to ras |
AU2351895A (en) | 1994-04-28 | 1995-11-29 | Yamanouchi Pharmaceutical Co., Ltd. | N-(3-pyrrolidinyl)benzamide derivative |
US5783568A (en) | 1994-06-10 | 1998-07-21 | Sugen, Inc. | Methods for treating cancer and other cell proliferative diseases |
JPH0823980A (en) | 1994-07-15 | 1996-01-30 | Terumo Corp | Nucleus receptor formed in apotosis of cerebral neurocyte and nucleus receptor gene coding the receptor |
EP1978033A3 (en) | 1995-04-27 | 2008-12-24 | Amgen Fremont Inc. | Human antibodies derived from immunized xenomice |
CA2219486A1 (en) | 1995-04-28 | 1996-10-31 | Abgenix, Inc. | Human antibodies derived from immunized xenomice |
US5958792A (en) | 1995-06-07 | 1999-09-28 | Chiron Corporation | Combinatorial libraries of substrate-bound cyclic organic compounds |
GB9525620D0 (en) | 1995-12-15 | 1996-02-14 | Glaxo Group Ltd | Chemical compounds |
EP0827742A1 (en) | 1996-09-04 | 1998-03-11 | Vrije Universiteit Brussel | Use of histone deacetylase inhibitors for treating fribosis or cirrhosis |
GB9821483D0 (en) | 1998-10-03 | 1998-11-25 | Glaxo Group Ltd | Chemical compounds |
JP3354090B2 (en) | 1996-09-30 | 2002-12-09 | シエーリング アクチエンゲゼルシャフト | Differentiation inducer |
US6174905B1 (en) | 1996-09-30 | 2001-01-16 | Mitsui Chemicals, Inc. | Cell differentiation inducer |
JP4215172B2 (en) | 1996-12-03 | 2009-01-28 | アムジェン フレモント インク. | Transgenic mammal having human Ig locus comprising a plurality of V {lower H} and V {lower κ} regions, and antibodies produced therefrom |
GB9625145D0 (en) | 1996-12-03 | 1997-01-22 | Smithkline Beecham Plc | Novel compounds |
JPH10330254A (en) | 1997-04-01 | 1998-12-15 | Kissei Pharmaceut Co Ltd | Suppressant for progress of pterygium and postoperative relapse |
US6444849B1 (en) | 1997-06-25 | 2002-09-03 | Mitsubishi Chemical Corporation | Amide derivatives |
CA2298480A1 (en) | 1997-07-25 | 1999-02-04 | Tsumura & Co. | Pyridylacrylamide derivatives and nephritis remedies and tgf-.beta. inhibitors containing the same |
ATE531812T1 (en) | 1997-12-05 | 2011-11-15 | Scripps Research Inst | HUMANIZATION OF RODENT ANTIBODIES |
US6140351A (en) | 1997-12-19 | 2000-10-31 | Berlex Laboratories, Inc. | Ortho-anthranilamide derivatives as anti-coagulants |
US6673827B1 (en) | 1999-06-29 | 2004-01-06 | The Uab Research Foundation | Methods of treating fungal infections with inhibitors of NAD synthetase enzyme |
JP4405602B2 (en) | 1998-04-16 | 2010-01-27 | バイエル・シエーリング・ファーマ アクチエンゲゼルシャフト | Histone deacetylase inhibitor |
HUP0102367A3 (en) | 1998-05-15 | 2002-11-28 | Astrazeneca Ab | Benzamide derivatives for the treatment of diseases mediated by cytokines |
DE69919212T2 (en) | 1998-12-23 | 2005-07-28 | Eli Lilly And Co., Indianapolis | AROMATIC AMIDES |
JP2000256194A (en) | 1999-01-06 | 2000-09-19 | Mitsui Chemicals Inc | Intranuclear receptor agonist and agent for enhancing its effect |
AU3857300A (en) | 1999-02-11 | 2000-08-29 | Cor Therapeutics, Inc. | Inhibitors of factor xa |
ATE303357T1 (en) | 1999-03-17 | 2005-09-15 | AMIDE DERIVATIVES | |
CA2366650A1 (en) | 1999-03-19 | 2000-09-28 | Michael Su | Oral low dose butyrate compositions |
JP2001081031A (en) | 1999-08-30 | 2001-03-27 | Schering Ag | Benzamide derivative-containing preparation having improved solubility and oral adsorption |
US6511990B1 (en) | 1999-09-08 | 2003-01-28 | Sloan-Kettering Institute For Cancer Research | Class of cytodifferentiating agents and histone deacetylase inhibitors, and methods of use thereof |
JP4360660B2 (en) | 1999-11-09 | 2009-11-11 | 三井化学株式会社 | Purification method of monoacylphenylenediamine derivatives |
WO2001042451A2 (en) | 1999-12-08 | 2001-06-14 | Genset | FULL-LENGTH HUMAN cDNAs ENCODING POTENTIALLY SECRETED PROTEINS |
TWI284639B (en) | 2000-01-24 | 2007-08-01 | Shionogi & Co | A compound having thrombopoietin receptor agonistic effect |
AU2001248701A1 (en) | 2000-03-24 | 2001-10-03 | Methylgene, Inc. | Inhibitors of histone deacetylase |
US7005439B2 (en) | 2000-06-20 | 2006-02-28 | Astrazeneca Ab | Compounds |
EP1170008A1 (en) | 2000-07-07 | 2002-01-09 | Chemotherapeutisches Forschungsinstitut Georg-Speyer-Haus | Valproic acid and derivatives thereof as histone deacetylase inhibitors |
DE60115279T2 (en) | 2000-09-29 | 2006-12-28 | Topotarget Uk Ltd., Abingdon | CARBOXIC ACID DERIVATIVES CONTAIN AN AMID GROUP AS HDAC INHIBITORS |
US20020103192A1 (en) | 2000-10-26 | 2002-08-01 | Curtin Michael L. | Inhibitors of histone deacetylase |
US6905669B2 (en) | 2001-04-24 | 2005-06-14 | Supergen, Inc. | Compositions and methods for reestablishing gene transcription through inhibition of DNA methylation and histone deacetylase |
US6897220B2 (en) | 2001-09-14 | 2005-05-24 | Methylgene, Inc. | Inhibitors of histone deacetylase |
US6706686B2 (en) | 2001-09-27 | 2004-03-16 | The Regents Of The University Of Colorado | Inhibition of histone deacetylase as a treatment for cardiac hypertrophy |
TW200304374A (en) | 2001-11-30 | 2003-10-01 | Smithkline Beecham Plc | Novel compounds |
US7993626B2 (en) | 2007-01-11 | 2011-08-09 | Immunomedics, Inc. | Methods and compositions for F-18 labeling of proteins, peptides and other molecules |
US20060089410A1 (en) | 2002-07-17 | 2006-04-27 | Titan Pharmaceuticals, Inc. | Combination of chemotherapeutic drugs for increasing antitumor activity |
US20050215601A1 (en) | 2002-09-25 | 2005-09-29 | Santen Pharmaceutical Co., Ltd. | Therapeutic agent for rheumatic disease comprising benzamide derivative as active ingredient |
US8163896B1 (en) | 2002-11-14 | 2012-04-24 | Rosetta Genomics Ltd. | Bioinformatically detectable group of novel regulatory genes and uses thereof |
US7790867B2 (en) | 2002-12-05 | 2010-09-07 | Rosetta Genomics Inc. | Vaccinia virus-related nucleic acids and microRNA |
US20050054647A1 (en) | 2002-12-27 | 2005-03-10 | Detlev Schuppan | New pharmaceutical combination |
US7244751B2 (en) | 2003-02-14 | 2007-07-17 | Shenzhen Chipscreen Biosciences Ltd. | Histone deacetylase inhibitors of novel benzamide derivatives with potent differentiation and anti-proliferation activity |
WO2005002626A2 (en) | 2003-04-25 | 2005-01-13 | Gilead Sciences, Inc. | Therapeutic phosphonate compounds |
PE20050206A1 (en) | 2003-05-26 | 2005-03-26 | Schering Ag | PHARMACEUTICAL COMPOSITION CONTAINING AN INHIBITOR OF HISTONE DEACETILASE |
TWI287010B (en) | 2003-06-12 | 2007-09-21 | Euro Celtique Sa | Therapeutic agents useful for treating pain |
US9005613B2 (en) | 2003-06-16 | 2015-04-14 | Immunomedics, Inc. | Anti-mucin antibodies for early detection and treatment of pancreatic cancer |
CN1284772C (en) | 2003-07-04 | 2006-11-15 | 深圳微芯生物科技有限责任公司 | Benzamide histone deacetylase inhibitor with differentiation and anti-proliferation activities and medicinal preparation thereof |
WO2005049105A2 (en) | 2003-11-10 | 2005-06-02 | Angiotech International Ag | Medical implants and anti-scarring agents |
US20130189364A1 (en) | 2004-07-09 | 2013-07-25 | Robert Sabin | Compositions and methods of potentiating adjuvant pharmaceuticals targeting latent viral infections |
EP2522396A1 (en) | 2005-02-03 | 2012-11-14 | TopoTarget UK Limited | Combination therapies using HDAC inhibitors |
US9707302B2 (en) | 2013-07-23 | 2017-07-18 | Immunomedics, Inc. | Combining anti-HLA-DR or anti-Trop-2 antibodies with microtubule inhibitors, PARP inhibitors, bruton kinase inhibitors or phosphoinositide 3-kinase inhibitors significantly improves therapeutic outcome in cancer |
SG160373A1 (en) | 2005-03-04 | 2010-04-29 | John Oaeneil | Adult pancreatic derived stromal cells |
AU2006244885B2 (en) * | 2005-05-09 | 2011-03-31 | E. R. Squibb & Sons, L.L.C. | Human monoclonal antibodies to programmed death 1(PD-1) and methods for treating cancer using anti-PD-1 antibodies alone or in combination with other immunotherapeutics |
WO2006135479A2 (en) | 2005-05-10 | 2006-12-21 | Angiotech International Ag | Anti-scarring agents, therapeutic compositions, and use thereof |
WO2006121521A2 (en) | 2005-05-10 | 2006-11-16 | Angiotech International Ag | Soft tissue implants, anti-scarring agents, and therapeutic compositions |
WO2006121522A2 (en) | 2005-05-10 | 2006-11-16 | Angiotech International Ag | Implantable sensors and pumps, anti-scarring agents, and therapeutic compositions |
US20090280153A1 (en) | 2005-05-10 | 2009-11-12 | Angiotech International Ag | electrical devices, anti-scarring agents, and therapeutic compositions |
EP1948195A2 (en) | 2005-11-17 | 2008-07-30 | Innate Pharma | Improved methods of using phosphoantigen for the treatment of cancer |
US20090247734A1 (en) | 2005-12-14 | 2009-10-01 | Hendrickson Wayne A | Chemically Derivatized CD4 and Uses Thereof |
EP2010916A2 (en) | 2006-04-13 | 2009-01-07 | Oncomethylome Sciences SA | Novel tumour suppressor |
WO2008012692A2 (en) | 2006-05-26 | 2008-01-31 | Methylgene Inc. | Assay for efficacy of histone deacetylase inhibitors |
EP2090577B1 (en) | 2006-10-19 | 2017-04-05 | Signal Pharmaceuticals, LLC | Heteroaryl compounds, compositions thereof, and their use as protein kinase inhibitors |
EA201201640A1 (en) | 2007-01-30 | 2013-09-30 | Фармасайкликс, Инк. | METHODS FOR DETERMINING CANCER STABILITY TO INHIBITORS HISTONEDEISETHYLASE |
CA2693707A1 (en) | 2007-07-13 | 2009-03-05 | The Johns Hopkins University | B7-dc variants |
US8088793B2 (en) | 2007-08-15 | 2012-01-03 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
CN101861151B (en) | 2007-09-14 | 2014-08-13 | 梅特希尔基因公司 | Cancer combination therapy with a selective inhibitor of histone deacetylase HDAC1, HDAC2 and/or HDAC3 and a microtubule stabilizer |
GB0802009D0 (en) | 2008-02-04 | 2008-03-12 | Chroma Therapeutics Ltd | Biomarkers of aminopeptidase inhibition |
JP2009209090A (en) | 2008-03-04 | 2009-09-17 | Mitsui Chemicals Inc | Insecticide, compound contained in the insecticide, and method of using the compound |
US9226934B2 (en) | 2008-06-02 | 2016-01-05 | The University Of Tokyo | Anti-cancer drug |
KR20110074850A (en) | 2008-08-25 | 2011-07-04 | 앰플리뮨, 인크. | PD-1 antagonists and methods of use thereof |
TWI453207B (en) | 2008-09-08 | 2014-09-21 | Signal Pharm Llc | Aminotriazolopyridines, compositions thereof, and methods of treatment therewith |
US20160041153A1 (en) | 2008-11-12 | 2016-02-11 | Kirk Brown | Biomarker compositions and markers |
CN101757626B (en) | 2008-12-26 | 2012-12-12 | 鼎泓国际投资(香港)有限公司 | Pharmaceutical composition containing insulin-like growth factor-I receptor inhibitor and histone deacetylase inhibitor and application thereof |
CN101756957B (en) | 2008-12-26 | 2012-11-14 | 鼎泓国际投资(香港)有限公司 | Pharmaceutical composition containing artemisinin, artemisinin derivatives and histone deacetylase inhibitor and application thereof |
CN101836989B (en) | 2009-03-19 | 2013-02-13 | 鼎泓国际投资(香港)有限公司 | Pharmaceutical composition containing tetrandrine, tetrandrine derivatives and histone deacetylase inhibitor and application thereof |
CN101837129B (en) | 2009-03-19 | 2012-12-12 | 鼎泓国际投资(香港)有限公司 | Pharmaceutical composition containing cMet inhibitor, HDAC inhibitor and EGFR tyrosine kinase inhibitor and application thereof |
US20160186266A1 (en) | 2009-10-27 | 2016-06-30 | Carislife Sciences, Inc. | Molecular profiling for personalized medicine |
JP2013510180A (en) | 2009-11-06 | 2013-03-21 | インフィニティ ファーマスーティカルズ、インク. | Oral formulation of hedgehog pathway inhibitor |
EP2499486A4 (en) | 2009-11-13 | 2013-11-27 | Infinity Pharmaceuticals Inc | Compositions, kits, and methods for identification, assessment, prevention, and therapy of cancer |
AU2010321773A1 (en) | 2009-11-20 | 2012-06-14 | Infinity Pharmaceuticals, Inc. | Methods and compositions for treating hedgehog-associated cancers |
LT2536706T (en) | 2010-02-11 | 2017-10-25 | Celgene Corporation | Arylmethoxy isoindoline derivatives and compositions comprising and methods of using the same |
NZ602634A (en) | 2010-03-26 | 2015-06-26 | Dartmouth College | Vista regulatory t cell mediator protein, vista binding agents and use thereof |
EP2556172A4 (en) | 2010-04-06 | 2013-10-30 | Caris Life Sciences Luxembourg Holdings | Circulating biomarkers for disease |
JO2998B1 (en) | 2010-06-04 | 2016-09-05 | Amgen Inc | Piperidinone derivatives as mdm2 inhibitors for the treatment of cancer |
US8993622B2 (en) | 2010-06-11 | 2015-03-31 | Eirium Ab | Antiviral compounds |
US20120010230A1 (en) | 2010-07-08 | 2012-01-12 | Macdougall John R | Methods and compositions for identification, assessment and treatment of cancers associated with hedgehog signaling |
WO2012006584A2 (en) | 2010-07-08 | 2012-01-12 | Infinity Pharmaceuticals, Inc. | Therapeutic regimens for hedgehog-associated cancers |
EP2606353A4 (en) | 2010-08-18 | 2014-10-15 | Caris Life Sciences Luxembourg Holdings | Circulating biomarkers for disease |
CN102441167B (en) | 2010-10-12 | 2014-05-07 | 鼎泓国际投资(香港)有限公司 | Pharmaceutical composition containing apigenin, apigenin derivatives and histone deacetylase inhibitors and application thereof |
US9808434B2 (en) | 2011-01-27 | 2017-11-07 | City Of Hope | Compound for treating cancer and diabetes |
EP2678448A4 (en) | 2011-02-22 | 2014-10-01 | Caris Life Sciences Luxembourg Holdings S A R L | Circulating biomarkers |
US20140349938A1 (en) | 2011-06-03 | 2014-11-27 | President And Fellows Of Harvard College | Methods of diagnosing and treating amyotrophic lateral sclerosis |
CN103782174A (en) | 2011-06-07 | 2014-05-07 | 卡里斯生命科学卢森堡控股有限责任公司 | Circulating biomarkers for cancer |
CN103797131A (en) | 2011-06-16 | 2014-05-14 | 卡里斯生命科学卢森堡控股有限责任公司 | Biomarker compositions and methods |
AU2012298794A1 (en) | 2011-08-23 | 2013-04-04 | Infinity Pharmaceuticals, Inc. | Biomarkers predictive of therapeutic responsiveness to HSP90 inhibitors and uses thereof |
WO2013039956A2 (en) | 2011-09-14 | 2013-03-21 | The Trustees Of Columbia University In The City Of New York | Compositions and methods for treating mood disorders |
PT2760471T (en) | 2011-09-30 | 2017-03-22 | Dana Farber Cancer Inst Inc | Therapeutic peptides |
EP2785683B1 (en) | 2011-11-30 | 2020-02-05 | Ludwig Institute for Cancer Research Ltd. | Inkt cell modulators and methods of using the same |
WO2013085902A1 (en) | 2011-12-05 | 2013-06-13 | The University Of Texas M.D. | Combination therapy methods for treating an inflammatory breast cancer |
IN2014KN00848A (en) | 2012-02-01 | 2015-10-02 | Compugen Ltd | |
WO2013124867A1 (en) | 2012-02-21 | 2013-08-29 | Amrita Vishwa Vidyapeetham University | Polymer - polymer or polymer - protein core - shell nano medicine loaded with multiple drug molecules |
WO2013134786A2 (en) | 2012-03-09 | 2013-09-12 | Caris Life Sciences Luxembourg Holdings, S.A.R.L. | Biomarker compositions and methods |
WO2013182661A1 (en) | 2012-06-06 | 2013-12-12 | Bionor Immuno As | Peptides derived from viral proteins for use as immunogens and dosage reactants |
EP2858665A1 (en) | 2012-06-06 | 2015-04-15 | Bionor Immuno AS | Vaccine |
WO2013190555A1 (en) | 2012-06-21 | 2013-12-27 | Compugen Ltd. | Lsr antibodies, and uses thereof for treatment of cancer |
US10258596B2 (en) | 2012-07-13 | 2019-04-16 | Gtx, Inc. | Method of treating HER2-positive breast cancers with selective androgen receptor modulators (SARMS) |
US10314807B2 (en) | 2012-07-13 | 2019-06-11 | Gtx, Inc. | Method of treating HER2-positive breast cancers with selective androgen receptor modulators (SARMS) |
ES2941477T3 (en) | 2012-08-13 | 2023-05-23 | Univ Rockefeller | LXRbeta agonist for cancer treatment |
US9382329B2 (en) | 2012-08-14 | 2016-07-05 | Ibc Pharmaceuticals, Inc. | Disease therapy by inducing immune response to Trop-2 expressing cells |
US9682143B2 (en) | 2012-08-14 | 2017-06-20 | Ibc Pharmaceuticals, Inc. | Combination therapy for inducing immune response to disease |
AU2013302696B9 (en) | 2012-08-14 | 2018-08-09 | Ibc Pharmaceuticals, Inc. | T-cell redirecting bispecific antibodies for treatment of disease |
CN104884065B (en) | 2012-09-21 | 2019-01-01 | 强烈治疗剂公司 | The method for the treatment of cancer |
EP2914722A1 (en) | 2012-11-05 | 2015-09-09 | Pronai Therapeutics, Inc. | Dosing and administration of oligonucleotide cancer therapies |
CN105051043B (en) | 2012-11-16 | 2017-05-10 | 默克专利有限公司 | Novel heterocyclic derivatives as modulators of kinase activity |
EP2922861A4 (en) | 2012-11-26 | 2016-09-14 | Caris Life Sciences Switzerland Holdings Gmbh | Biomarker compositions and methods |
CN103833626B (en) | 2012-11-27 | 2015-11-25 | 深圳微芯生物科技有限责任公司 | Crystal formation of chidamide and preparation method thereof and application |
ES2821102T3 (en) | 2012-11-29 | 2021-04-23 | Merck Patent Gmbh | Azaquinazolinecarboxamide derivatives |
ES2819573T3 (en) | 2012-12-13 | 2021-04-16 | Immunomedics Inc | Method for Producing Antibody-SN-38 Immunoconjugates with a CL2A Linker |
CN107753954A (en) | 2012-12-13 | 2018-03-06 | 免疫医疗公司 | The dosage of the antibody that effect is improved and toxicity reduces and SN 38 immunoconjugates |
US10137196B2 (en) | 2012-12-13 | 2018-11-27 | Immunomedics, Inc. | Dosages of immunoconjugates of antibodies and SN-38 for improved efficacy and decreased toxicity |
US9492566B2 (en) | 2012-12-13 | 2016-11-15 | Immunomedics, Inc. | Antibody-drug conjugates and uses thereof |
RU2644411C2 (en) | 2013-02-07 | 2018-02-12 | Филипс Лайтинг Холдинг Б.В. | Lighting system having controller that supports selected light scene, and method for controlling such system |
CN105209068A (en) | 2013-02-07 | 2015-12-30 | 免疫医疗公司 | Pro-drug form (P2PDox) of the highly potent 2-pyrrolinodoxorubicin conjugated to antibodies for targeted therapy of cancer |
CN104056270B (en) | 2013-02-21 | 2018-11-09 | 中国人民解放军军事医学科学院野战输血研究所 | It is used to prepare the histon deacetylase (HDAC) inhibitor that multiple organ injury gives treatment to drug |
EP2964648B1 (en) | 2013-03-05 | 2016-11-16 | Merck Patent GmbH | 9-(aryl or heteroaryl)-2-(pyrazolyl, pyrrolidinyl or cyclopentyl)aminopurine derivatives as anticancer agents |
EP2964649B1 (en) | 2013-03-05 | 2017-05-10 | Merck Patent GmbH | Triazolo[4,5-d]pyrimidine derivatives for the treatment of diseases such as cancer |
WO2014151899A1 (en) | 2013-03-14 | 2014-09-25 | Seragon Pharmaceuticals, Inc. | Polycyclic estrogen receptor modulators and uses thereof |
PL2970473T3 (en) | 2013-03-14 | 2018-01-31 | Bristol Myers Squibb Co | Combination of dr5 agonist and anti-pd-1 antagonist and methods of use |
AR095363A1 (en) | 2013-03-15 | 2015-10-14 | Genentech Inc | BIOMARKERS AND METHODS FOR THE TREATMENT OF CONDITIONS RELATED TO PD-1 AND PD-L1 |
EP3666886A1 (en) | 2013-03-15 | 2020-06-17 | Dana-Farber Cancer Institute, Inc. | Therapeutic peptides |
US9308236B2 (en) | 2013-03-15 | 2016-04-12 | Bristol-Myers Squibb Company | Macrocyclic inhibitors of the PD-1/PD-L1 and CD80(B7-1)/PD-L1 protein/protein interactions |
EP2970965A2 (en) | 2013-03-15 | 2016-01-20 | Pronai Therapeutics, Inc. | Dnai for the modulation of genes |
CN104069106A (en) | 2013-03-27 | 2014-10-01 | 南通瑞思医药技术有限公司 | Application of benzamide compound in preparation of medicine for activating latent human immunodeficiency virus |
WO2014172637A1 (en) | 2013-04-18 | 2014-10-23 | Immune Design Corp. | Gla monotherapy for use in cancer treatment |
JP2016519166A (en) | 2013-05-24 | 2016-06-30 | クーパー ヒューマン システムズ エルエルシー | Methods and compositions for treating HIV infection |
WO2014193999A2 (en) | 2013-05-28 | 2014-12-04 | Caris Science, Inc. | Biomarker methods and compositions |
BR112015030595A2 (en) | 2013-06-19 | 2017-07-25 | Seragon Pharmaceuticals Inc | azetidine estrogen receptor modulators and uses thereof |
AU2014281511A1 (en) | 2013-06-19 | 2015-12-03 | Seragon Pharmaceuticals, Inc. | Estrogen receptor modulator and uses thereof |
ES2661437T3 (en) | 2013-06-21 | 2018-04-02 | Zenith Epigenetics Corp. | New substituted bicyclic compounds as bromodomain inhibitors |
WO2015007337A1 (en) | 2013-07-19 | 2015-01-22 | Bionor Immuno As | Method for the vaccination against hiv |
WO2015013579A1 (en) | 2013-07-26 | 2015-01-29 | Update Pharma Inc. | Compositions to improve the therapeutic benefit of bisantrene |
BR112016001978A2 (en) | 2013-07-29 | 2017-08-01 | Merck Patent Gmbh | 1,3-disubstituted cyclopentane derivatives |
WO2015017546A1 (en) | 2013-07-30 | 2015-02-05 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Selective histone deactylase 6 inhibitors |
MX359656B (en) | 2013-07-31 | 2018-10-05 | Merck Patent Gmbh | Oxoquinazolinyl-butanamide derivatives. |
EA201690087A1 (en) | 2013-07-31 | 2016-08-31 | Зенит Эпидженетикс Корп. | NEW QUINAZOLINONS AS BROMOMODENIAL INHIBITORS |
WO2015019284A2 (en) | 2013-08-05 | 2015-02-12 | Cambridge Enterprise Limited | Inhibition of cxcr4 signaling in cancer immunotherapy |
MX366140B (en) | 2013-08-07 | 2019-06-27 | Merck Patent Gmbh | Piperidine urea derivatives. |
WO2015023938A1 (en) | 2013-08-16 | 2015-02-19 | Rana Therapeutics, Inc. | Epigenetic regulators of frataxin |
CN103432077A (en) | 2013-08-21 | 2013-12-11 | 北京淦航医药科技有限公司 | Chidamide solid dispersion preparation |
US10966998B2 (en) | 2013-09-05 | 2021-04-06 | The Johns Hopkins University | Cancer therapy via a combination of epigenetic modulation and immune modulation |
US20160272707A1 (en) | 2013-09-11 | 2016-09-22 | Compugen Ltd. | Vstm5 antibodies, and uses thereof for treatment of cancer, infectious diseases and immune related diseases |
WO2015037000A1 (en) | 2013-09-11 | 2015-03-19 | Compugen Ltd | Vstm5 polypeptides and uses thereof as a drug for treatment of cancer, infectious diseases and immune related diseases |
WO2015048547A2 (en) | 2013-09-26 | 2015-04-02 | Rigel Pharmaceuticals, Inc. | Methods for using and biomarkers for ampk-activating compounds |
US20150094518A1 (en) | 2013-09-27 | 2015-04-02 | The Regents Of The University Of California | Modular polymer platform for the treatment of cancer |
EP3060654B1 (en) | 2013-10-21 | 2023-03-15 | Hemoshear, LLC | In vitro model for a tumor microenvironment |
MX2016005054A (en) | 2013-10-21 | 2016-07-19 | Merck Patent Gmbh | Heteroaryl compounds as btk inhibitors and uses thereof. |
US20170080093A1 (en) | 2013-10-22 | 2017-03-23 | Tyme, Inc. | Tyrosine Derivatives And Compositions Comprising Them |
PE20160546A1 (en) | 2013-10-25 | 2016-05-26 | Novartis Ag | BICYCLE PYRIDYL DERIVED COMPOUNDS FUSED TO RING AS INHIBITORS OF FGFR4 |
CN108464981B (en) | 2013-11-07 | 2022-06-24 | 德西费拉制药有限责任公司 | Use of composition for inhibiting TIE2 kinase in preparing medicine for treating cancer |
US9457019B2 (en) | 2013-11-07 | 2016-10-04 | Deciphera Pharmaceuticals, Llc | Methods for inhibiting tie-2 kinase useful in the treatment of cancer |
EP3068443B1 (en) | 2013-11-12 | 2019-04-10 | Centre for Probe Development and Commercialization | Residualizing linkers and uses thereof |
US20150140036A1 (en) | 2013-11-13 | 2015-05-21 | Novartis Institutes For Biomedical Research, Inc. | Low, immune enhancing, dose mtor inhibitors and uses thereof |
NZ720004A (en) | 2013-11-18 | 2020-03-27 | Forma Therapeutics Inc | Tetrahydroquinoline compositions as bet bromodomain inhibitors |
EP3071205B1 (en) | 2013-11-18 | 2020-02-05 | Forma Therapeutics, Inc. | Benzopiperazine compositions as bet bromodomain inhibitors |
WO2015077717A1 (en) | 2013-11-25 | 2015-05-28 | The Broad Institute Inc. | Compositions and methods for diagnosing, evaluating and treating cancer by means of the dna methylation status |
KR20160090904A (en) | 2013-12-06 | 2016-08-01 | 다나-파버 캔서 인스티튜트 인크. | Therapeutic peptides |
WO2015086738A2 (en) | 2013-12-11 | 2015-06-18 | Bionor Immuno As | Hiv vaccine |
WO2015089380A2 (en) | 2013-12-12 | 2015-06-18 | Celcuity Llc | Assays and methods for determining the responsiveness of an individual subject to a therapeutic agent |
US20160263092A1 (en) | 2013-12-19 | 2016-09-15 | Twi Biotechnology, Inc. | Therapeutic uses of berberine formulations |
JP7060324B2 (en) | 2013-12-20 | 2022-04-26 | ザ・ブロード・インスティテュート・インコーポレイテッド | Combination therapy with neoantigen vaccine |
MY186311A (en) | 2013-12-20 | 2021-07-08 | Astex Therapeutics Ltd | Bicyclic heterocycle compounds and their uses in therapy |
HUE037606T2 (en) | 2013-12-23 | 2018-09-28 | Merck Patent Gmbh | Imidazopyrazinone derivatives |
WO2015096982A1 (en) | 2013-12-23 | 2015-07-02 | Bayer Pharma Aktiengesellschaft | Antibody drug conjugates (adcs) with kinesin spindel protein (ksp) |
AU2015204572B2 (en) | 2014-01-10 | 2020-07-30 | Inspirna, Inc. | LXR agonists and uses thereof |
CN104771363A (en) | 2014-01-14 | 2015-07-15 | 深圳微芯生物科技有限责任公司 | Chidamide solid dispersion and preparing method and application thereof |
JOP20200094A1 (en) | 2014-01-24 | 2017-06-16 | Dana Farber Cancer Inst Inc | Antibody Molecules of PD-1 and Their Uses |
US10143737B2 (en) | 2014-01-27 | 2018-12-04 | Bionor Pharma Asa | Method for the vaccination against HIV |
CA2936335A1 (en) | 2014-01-27 | 2015-07-30 | Bionor Immuno As | Dosage regimen for hiv vaccine |
WO2015110659A1 (en) | 2014-01-27 | 2015-07-30 | Bionor Immuno As | Methods of immunization with a vaccine inducing a humoral immune response and with a vaccine inducing a cellular immune response |
US9631013B2 (en) | 2014-01-28 | 2017-04-25 | Fibrogen, Inc. | Therapeutic method for pancreatic cancer |
WO2015113927A1 (en) | 2014-01-29 | 2015-08-06 | Bayer Pharma Aktiengesellschaft | Amino-substituted isothiazoles |
EP3099682A1 (en) | 2014-01-29 | 2016-12-07 | Bayer Pharma Aktiengesellschaft | Amino-substituted isothiazoles |
JOP20200096A1 (en) | 2014-01-31 | 2017-06-16 | Children’S Medical Center Corp | Antibody molecules to tim-3 and uses thereof |
WO2015120382A1 (en) | 2014-02-07 | 2015-08-13 | The Johns Hopkins University | Predicting response to epigenetic drug therapy |
JP6577479B2 (en) | 2014-02-27 | 2019-09-18 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | Heterocyclic compounds and their use as NAV channel inhibitors |
WO2015127548A1 (en) | 2014-02-28 | 2015-09-03 | The Royal Institution For The Advancement Of Learning / Mcgill University | Tc-ptp inhibitors as apc activators for immunotherapy |
MX2016011612A (en) | 2014-03-11 | 2016-12-12 | The Council Of The Queensland Inst Of Medical Res | Determining cancer agressiveness, prognosis and responsiveness to treatment. |
EP3116496A1 (en) | 2014-03-13 | 2017-01-18 | F. Hoffmann-La Roche AG | Methods and compositions for modulating estrogen receptor mutants |
EP3116497A2 (en) | 2014-03-13 | 2017-01-18 | F. Hoffmann-La Roche AG | Therapeutic combinations with estrogen receptor modulators |
ME03558B (en) | 2014-03-14 | 2020-07-20 | Novartis Ag | Antibody molecules to lag-3 and uses thereof |
JP6701088B2 (en) | 2014-03-19 | 2020-05-27 | インフィニティー ファーマシューティカルズ, インコーポレイテッド | Heterocyclic compounds for use in the treatment of PI3K-gamma mediated disorders |
UY36060A (en) | 2014-04-02 | 2015-10-30 | Bayer Pharma AG | AZOL COMPOUNDS REPLACED WITH AMIDA |
CN104974079A (en) | 2014-04-02 | 2015-10-14 | C&C生物医药有限公司 | Amide derivatives of aniline-related compound and composition of amide derivatives of aniline-related compound |
US12146874B2 (en) | 2014-04-03 | 2024-11-19 | University Of Maryland, Baltimore | Microtentacle imaging in patient tumor samples |
CN103880736B (en) | 2014-04-04 | 2017-05-17 | 深圳微芯生物科技有限责任公司 | E-configuration benzamide compounds, and pharmaceutical preparation application thereof |
JP6767875B2 (en) | 2014-04-08 | 2020-10-14 | ライジェル ファーマシューティカルズ, インコーポレイテッド | 2,3-Disubstituted pyridine compound as a TGF-beta inhibitor and how to use it |
NO2776305T3 (en) | 2014-04-23 | 2018-01-27 | ||
JP2015209376A (en) | 2014-04-24 | 2015-11-24 | 国立大学法人北海道大学 | Tumor-specific immuno-enhancing agent |
EP3137447B1 (en) | 2014-04-30 | 2021-06-30 | Rgenix, Inc. | Inhibitors of creatine transport and uses thereof |
WO2015168614A2 (en) | 2014-05-01 | 2015-11-05 | Board Of Regents Of The University Of Nebraska | Polymer compositions of histone deacetylase inhibitors and methods of use thereof |
WO2015172747A1 (en) | 2014-05-16 | 2015-11-19 | Zhaoyin Wang | Spirocyclic molecules as mth1 inhibitors |
GB201409471D0 (en) | 2014-05-28 | 2014-07-09 | Euro Celtique Sa | Pharmaceutical composition |
PL3155017T4 (en) | 2014-05-28 | 2024-06-17 | Mederis Diabetes, Llc | Improved peptide pharmaceuticals for insulin resistance |
WO2015184405A1 (en) | 2014-05-30 | 2015-12-03 | Medivation Technologies, Inc. | Aromatic compounds, compositions and uses thereof |
WO2015191568A2 (en) | 2014-06-09 | 2015-12-17 | Biomed Valley Discoveries, Inc. | Combination therapies using agents that target tumor-associated stroma or tumor cells and tumor vasculature |
TWI729644B (en) | 2014-06-12 | 2021-06-01 | 美商西爾拉癌症醫學公司 | N-(cyanomethyl)-4-(2-(4-morpholinophenylamino)pyrimidin-4-yl)benzamide |
US10221197B2 (en) | 2014-06-13 | 2019-03-05 | Gilead Sciences, Inc. | Phosphatidylinositol 3-kinase inhibitors |
SG11201609527PA (en) | 2014-06-13 | 2016-12-29 | Gilead Sciences Inc | Quinazolinone derivatives as phosphatidylinositol 3-kinase inhibitors |
EA201692265A1 (en) | 2014-06-13 | 2017-05-31 | Джилид Сайэнс, Инк. | PHOSPHATIDYLINOSITOL-3-KINASE INHIBITORS |
JP6454736B2 (en) | 2014-06-13 | 2019-01-16 | ギリアード サイエンシーズ, インコーポレイテッド | Phosphatidylinositol 3-kinase inhibitor |
EP3154960A1 (en) | 2014-06-13 | 2017-04-19 | Gilead Sciences, Inc. | Phosphatidylinositol 3-kinase inhibitors |
ES2769648T3 (en) | 2014-06-16 | 2020-06-26 | Fundacion Para La Investig Medica Aplicada | Novel compounds as dual inhibitors of histone methyltransferases and DNA methyltransferases ASAS |
CA2952307A1 (en) | 2014-06-17 | 2015-12-23 | Bayer Pharma Aktiengesellschaft | 3-amino-1,5,6,7-tetrahydro-4h-indol-4-ones |
NO2717902T3 (en) | 2014-06-20 | 2018-06-23 | ||
TW201613936A (en) | 2014-06-20 | 2016-04-16 | Gilead Sciences Inc | Crystalline forms of(2R,5S,13aR)-8-hydroxy-7,9-dioxo-n-(2,4,6-trifluorobenzyl)-2,3,4,5,7,9,13,13a-octahydro-2,5-methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide |
SG11201610341PA (en) | 2014-06-24 | 2017-01-27 | Gilead Sciences Inc | Phosphatidylinositol 3-kinase inhibitors |
WO2015200790A2 (en) | 2014-06-26 | 2015-12-30 | Yale University | Compositions and methods to regulate renalase in the treatment of diseases and disorders |
US20170165321A1 (en) | 2014-07-11 | 2017-06-15 | Bionor Immuno As | Method for reducing and/or delaying pathological effects of human immunodeficiency virus i (hiv) or for reducing the risk of developing acquired immunodeficiency syndrome (aids) |
PL3166607T3 (en) | 2014-07-11 | 2023-02-20 | Gilead Sciences, Inc. | Modulators of toll-like receptors for the treatment of hiv |
CN114099686B (en) | 2014-07-15 | 2024-04-16 | 约翰·霍普金斯大学 | Inhibition of myeloid-derived suppressor cells and immune checkpoint blockade |
CN104083763A (en) | 2014-07-16 | 2014-10-08 | 中国人民解放军军事医学科学院野战输血研究所 | Application of histone deacetylase inhibitor in preparation of latent virus activator |
AU2015289044A1 (en) | 2014-07-17 | 2016-12-08 | Cancer Research Technology Limited | Novel naphthryidines and isoquinolines and their use as CDK8/19 inhibitors |
WO2016014890A1 (en) | 2014-07-24 | 2016-01-28 | Calithera Biosciences, Inc. | Treatment of multiple myeloma with heterocyclic inhibitors of glutaminase |
JP2017522332A (en) | 2014-07-25 | 2017-08-10 | バイエル ファーマ アクチエンゲゼルシャフト | Amino-substituted isoxazoles |
WO2016018920A1 (en) | 2014-07-29 | 2016-02-04 | Admune Therapeutics Llc | Il-15 and il-15ralpha heterodimer dose escalation regimens for treating conditions |
TWI700283B (en) | 2014-08-04 | 2020-08-01 | 德商拜耳製藥公司 | 2-(morpholin-4-yl)-1,7-naphthyridines |
EP4180041A1 (en) | 2014-08-07 | 2023-05-17 | Mayo Foundation for Medical Education and Research | Compounds and methods for treating cancer |
GB201414464D0 (en) | 2014-08-14 | 2014-10-01 | Technion Res & Dev Foundation | Compositions and methods for therapeutics prescreening |
MX2017002199A (en) | 2014-08-18 | 2017-08-18 | Ono Pharmaceutical Co | ACID-ADDITION SALT OF Trk-INHIBITING COMPOUND. |
JO3663B1 (en) | 2014-08-19 | 2020-08-27 | Merck Sharp & Dohme | Anti-lag3 antibodies and antigen-binding fragments |
US10912933B2 (en) | 2014-08-19 | 2021-02-09 | The Regents Of The University Of California | Implants for localized drug delivery and methods of use thereof |
US20170231931A1 (en) | 2014-08-26 | 2017-08-17 | Fundación Para La Investigación Médica Aplicada | Products for the treatment and prevention of neurological disorders coursing with a cognition deficit or impairment, and of neurodegenerative diseases |
JP6491321B2 (en) | 2014-08-29 | 2019-03-27 | ギリアード サイエンシーズ, インコーポレイテッド | Antiretroviral agent |
WO2016036759A1 (en) | 2014-09-04 | 2016-03-10 | Gilead Sciences, Inc. | Methods of treating or preventing hiv in patients using a combination of tenofovir alafenamide and dolutegravir |
RU2718914C2 (en) | 2014-09-13 | 2020-04-15 | Новартис Аг | Combined treatment methods using alk inhibitors |
SI3194401T1 (en) | 2014-09-16 | 2020-12-31 | Gilead Sciences, Inc. | Solid forms of a toll-like receptor modulator |
JP2017529353A (en) | 2014-09-19 | 2017-10-05 | バイエル ファーマ アクチエンゲゼルシャフト | Benzyl-substituted indazoles as Bub1 kinase inhibitors |
WO2016042080A1 (en) | 2014-09-19 | 2016-03-24 | Bayer Pharma Aktiengesellschaft | Benzyl substituted indazoles as bub1 kinase inhibitors |
BR112017005444A2 (en) | 2014-09-19 | 2018-04-24 | Bayer Pharma AG | benzyl substituted indazoles as bub1 inhibitors. |
CN107148420A (en) | 2014-09-19 | 2017-09-08 | 拜耳制药股份公司 | The indazole compounds of benzyl substitution |
EP3194368B1 (en) | 2014-09-19 | 2020-12-23 | MacKay Medical Foundation the Presbyterian Church in Taiwan MacKay Memorial Hospital | Benzo-heterocyclic compounds and their applications |
EP3198276B1 (en) | 2014-09-24 | 2023-09-20 | Exscientia GmbH | Monolayer of pbmcs or bone-marrow cells and uses thereof |
CN104530415B (en) | 2014-10-01 | 2017-09-01 | 厦门赛诺邦格生物科技股份有限公司 | A kind of different functionalization Y types polyethyleneglycol derivative, preparation method and its bio-related substance |
CN104530413B (en) | 2014-10-01 | 2017-08-25 | 厦门赛诺邦格生物科技股份有限公司 | A kind of bio-related substance of multiple functionalized H types polyethyleneglycol derivative modification |
CN104725628B (en) | 2014-10-01 | 2018-04-17 | 厦门赛诺邦格生物科技股份有限公司 | A kind of single functionalization branched polyethylene glycol, preparation method and its bio-related substance containing degradable group |
CA2963281A1 (en) | 2014-10-03 | 2016-04-07 | Novartis Ag | Combination therapies |
US9446148B2 (en) | 2014-10-06 | 2016-09-20 | Mayo Foundation For Medical Education And Research | Carrier-antibody compositions and methods of making and using the same |
AU2015328285B2 (en) | 2014-10-06 | 2019-07-18 | Merck Patent Gmbh | Heteroaryl compounds as BTK inhibitors and uses thereof |
US9732119B2 (en) | 2014-10-10 | 2017-08-15 | Bristol-Myers Squibb Company | Immunomodulators |
CN107001478B (en) | 2014-10-14 | 2022-01-11 | 诺华股份有限公司 | Antibody molecules against PD-L1 and uses thereof |
CN107106638A (en) | 2014-10-14 | 2017-08-29 | 激流生物科学有限公司 | Peptide with anti-inflammatory property |
WO2016061495A1 (en) | 2014-10-16 | 2016-04-21 | Predictive Therapeutics Ltd. | Atavarsitic systems and methods for biomarker discovery |
WO2016065349A2 (en) | 2014-10-24 | 2016-04-28 | University Of Maryland, Baltimore | Short non-coding protein regulatory rnas (sprrnas) and methods of use |
EP3212228A2 (en) | 2014-10-27 | 2017-09-06 | Ruprecht-Karls-Universität Heidelberg | Use of ccr5 antagonists alone or in combination therapy for the treatment of cancer |
DK3643709T3 (en) | 2014-10-30 | 2021-12-20 | Kangpu Biopharmaceuticals Inc | ISOINDOLINE DERIVATIVE, INTERMEDIATE PRODUCT, METHOD OF MANUFACTURE, PHARMACEUTICAL COMPOSITION AND USE |
WO2016070089A2 (en) | 2014-10-31 | 2016-05-06 | Abbvie Biotherapeutics Inc. | Anti-cs1 antibodies and antibody drug conjugates |
WO2016070051A2 (en) | 2014-10-31 | 2016-05-06 | Oncomed Pharmaceuticals, Inc. | Combination therapy for treatment of disease |
EP3215182B1 (en) | 2014-11-05 | 2023-01-04 | The Regents of The University of California | Combination immunotherapy |
WO2016071477A1 (en) | 2014-11-07 | 2016-05-12 | Rheinische Friedrich-Wilhelms-Universität Bonn Institut Für Rekonstruktive Neurobiologie | Methods for assessing the treatment response of cancer patients and for treating cancer patients by analysing cpg methylation |
CA2967188A1 (en) | 2014-11-14 | 2016-05-19 | Novartis Ag | Antibody drug conjugates |
US9856292B2 (en) | 2014-11-14 | 2018-01-02 | Bristol-Myers Squibb Company | Immunomodulators |
ES2978534T3 (en) | 2014-11-17 | 2024-09-13 | Cellectar Biosciences Inc | Phospholipid ether analogues as anticancer drug carriers |
WO2016081384A1 (en) * | 2014-11-17 | 2016-05-26 | Genentech, Inc. | Combination therapy comprising ox40 binding agonists and pd-1 axis binding antagonists |
US10526341B2 (en) | 2014-11-19 | 2020-01-07 | Memorial Sloan-Kettering Cancer Center | Thienopyrimidines and uses thereof |
US9790221B2 (en) | 2014-11-20 | 2017-10-17 | Merck Patent Gmbh | Heteroaryl compounds as IRAK inhibitors and uses thereof |
WO2016087936A1 (en) | 2014-12-01 | 2016-06-09 | Zenith Epigenetics Corp. | Substituted pyridinones as bromodomain inhibitors |
WO2016089928A1 (en) | 2014-12-01 | 2016-06-09 | Weitz Andrew C | Methods for treating and assessing tumor invasion and metastasis |
WO2016087942A1 (en) | 2014-12-01 | 2016-06-09 | Zenith Epigenetics Corp. | Substituted pyridines as bromodomain inhibitors |
WO2016087490A1 (en) | 2014-12-03 | 2016-06-09 | Bayer Pharma Aktiengesellschaft | Combination of pi3k-inhibitors |
WO2016087488A1 (en) | 2014-12-03 | 2016-06-09 | Bayer Pharma Aktiengesellschaft | Administration regime for aminoalcohol substituted 2,3-dihydroimidazo[1,2-c]quinazoline derivatives |
JP2018500930A (en) | 2014-12-04 | 2018-01-18 | アブルッツォ・セラノスティックス・エッセ・エッレ・エッレ | Humanized anti-TROP-2 monoclonal antibody and use thereof |
CA2968352A1 (en) | 2014-12-08 | 2016-06-16 | Dana-Farber Cancer Institute, Inc. | Methods for upregulating immune responses using combinations of anti-rgmb and anti-pd-1 agents |
HUE055290T2 (en) | 2014-12-09 | 2021-11-29 | Bayer Ag | Benzamide derivatives substituted with 1,3-thiazol-2-yl |
WO2016094309A1 (en) | 2014-12-10 | 2016-06-16 | Myosotis | Inhibition of tnf signaling in cancer immunotherapy |
US20170343554A1 (en) | 2014-12-12 | 2017-11-30 | Celcuity Llc | Methods of measuring erbb signaling pathway activity to diagnose and treat cancer patients |
EP3233127A1 (en) | 2014-12-15 | 2017-10-25 | Bayer Pharma Aktiengesellschaft | Antibody-drug conjugates (adcs) of ksp inhibitors with aglycosylated anti-tweakr antibodies |
WO2016100619A2 (en) | 2014-12-17 | 2016-06-23 | Rgenix, Inc. | Treatment and diagnosis of cancer |
US9845291B2 (en) | 2014-12-18 | 2017-12-19 | Genentech, Inc. | Estrogen receptor modulators and uses thereof |
US9861680B2 (en) | 2014-12-18 | 2018-01-09 | Bristol-Myers Squibb Company | Immunomodulators |
US20160175284A1 (en) | 2014-12-18 | 2016-06-23 | Genentech, Inc. | Estrogen receptor modulators and uses thereof |
US10172814B2 (en) | 2014-12-18 | 2019-01-08 | Bayer Pharma Aktiengesellschaft | Substituted pyridyl-cycloalkyl-carboxylic acids, compositions containing them and medical uses thereof |
IL311006A (en) | 2014-12-18 | 2024-04-01 | Hoffmann La Roche | TETRAHYDRO-PYRIDO[3,4-b]INDOLE ESTROGEN RECEPTOR MODULATORS AND USES THEREOF |
US9944678B2 (en) | 2014-12-19 | 2018-04-17 | Bristol-Myers Squibb Company | Immunomodulators |
EP3233918A1 (en) | 2014-12-19 | 2017-10-25 | Novartis AG | Combination therapies |
ES2724367T3 (en) | 2014-12-19 | 2019-09-10 | Epigenomics Ag | Methods to detect CpG methylation and to diagnose cancer |
WO2016100975A1 (en) | 2014-12-19 | 2016-06-23 | Massachsetts Institute Ot Technology | Molecular biomarkers for cancer immunotherapy |
WO2016102493A1 (en) | 2014-12-22 | 2016-06-30 | Bayer Pharma Aktiengesellschaft | Imidazopyridine ezh2 inhibitors |
DE102014226903A1 (en) | 2014-12-23 | 2016-06-23 | Olympus Winter & Ibe Gmbh | RF adjuvant, medical system and method for selectively treating cancerous tissue |
WO2016102427A1 (en) | 2014-12-23 | 2016-06-30 | Bayer Pharma Aktiengesellschaft | 6-hydroxybenzofuranyl- and 6-alkoxybenzofuranyl-substituted imidazopyridazines |
TWI695003B (en) | 2014-12-23 | 2020-06-01 | 美商基利科學股份有限公司 | Polycyclic-carbamoylpyridone compounds and their pharmaceutical use |
CN107207472B (en) | 2014-12-23 | 2020-08-14 | 卑尔根生物股份公司 | Inhibitors of AKT kinase |
TWI699355B (en) | 2014-12-24 | 2020-07-21 | 美商基利科學股份有限公司 | Quinazoline compounds |
NZ733125A (en) | 2014-12-24 | 2018-06-29 | Gilead Sciences Inc | Isoquinoline compounds for the treatment of hiv |
BR112017013491A2 (en) | 2014-12-24 | 2018-01-09 | Gilead Sciences, Inc. | fused pyrimidine compounds for the treatment of hiv |
US20160200815A1 (en) | 2015-01-05 | 2016-07-14 | Jounce Therapeutics, Inc. | Antibodies that inhibit tim-3:lilrb2 interactions and uses thereof |
EP3242671A4 (en) | 2015-01-08 | 2018-08-08 | Hackensack University Medical Center | Ex vivo methods for minimizing risks and maximizing benefits of allogeneic blood and marrow transplantation |
EP3693022A3 (en) | 2015-01-09 | 2020-09-16 | Reiley Pharmaceuticals, Inc. | Cox-2-targeting, platinum-containing conjugates and their use in the treatment of tumors and cancers |
WO2016117666A1 (en) | 2015-01-23 | 2016-07-28 | 国立大学法人鹿児島大学 | Agent for killing hiv-1-infected cell and application thereof |
EP3247353A4 (en) | 2015-01-23 | 2018-07-04 | Confluence Life Sciences, Inc. | Heterocyclic itk inhibitors for treating inflammation and cancer |
SG11201705908VA (en) | 2015-01-28 | 2017-08-30 | Bayer Pharma AG | 4h-pyrrolo[3,2-c]pyridin-4-one derivatives |
PL3250208T3 (en) | 2015-01-30 | 2021-04-06 | Oncoceutics, Inc. | 7-BENZYLO-4- (4- (TRIFLUOROMETHYL) BENZYLO) -1,2,6,7,8,9-HEXAHYDROIMIDAZO [1,2-A] PYRIDO [3,4-E] PYRIMIDIN-5 (4H) - HE AND HIS SALTS AND THEIR APPLICATION IN THERAPY |
TW201639573A (en) | 2015-02-03 | 2016-11-16 | 吉李德科學股份有限公司 | Combination therapies for treating cancers |
US20160222060A1 (en) | 2015-02-04 | 2016-08-04 | Bristol-Myers Squibb Company | Immunomodulators |
EP3253764B1 (en) | 2015-02-05 | 2021-06-09 | Merck Patent GmbH | Macrocyclic compounds as irak1/4 inhibitors and uses thereof |
CA2970550C (en) | 2015-02-06 | 2023-09-19 | Merck Patent Gmbh | Pyridazinone macrocycles as irak inhibitors and uses thereof |
MY193968A (en) | 2015-02-12 | 2022-11-03 | Beyondspring Pharmaceuticals Inc | Use of plinabulin in combination with immune checkpoint inhibitors |
WO2016133910A1 (en) | 2015-02-17 | 2016-08-25 | Cantex Pharmaceuticals, Inc. | Treatment of cancers and hematopoietic stem cell disorders privileged by cxcl12-cxcr4 interaction |
WO2016133194A1 (en) | 2015-02-20 | 2016-08-25 | 第一三共株式会社 | Combination method for treating cancer |
MY186133A (en) | 2015-03-02 | 2021-06-24 | Rigel Pharmaceuticals Inc | Tgf-? inhibitors |
KR101756050B1 (en) | 2015-03-04 | 2017-07-07 | 길리애드 사이언시즈, 인코포레이티드 | Toll like receptor modulator compounds |
US20180042929A1 (en) | 2015-03-09 | 2018-02-15 | Bayer Pharma Aktiengesellschaft | Use of substituted 2,3-dihydroimidazo[1,2-c]quinazolines |
BR112017019188A2 (en) | 2015-03-09 | 2018-04-24 | Bayer Pharma Aktiengesellschaft | COMBINATIONS CONTAINING 2,3-DI-HYDROIMIDAZO [1,2-C] REPLACED QUINAZOLINE |
WO2016145150A2 (en) | 2015-03-11 | 2016-09-15 | The Broad Institute Inc. | Selective treatment of prmt5 dependent cancer |
EP3988106A1 (en) | 2015-03-13 | 2022-04-27 | Ospedale San Raffaele S.r.l. | Il-10-producing cd4+ t cells and uses thereof |
US10195237B2 (en) | 2015-03-16 | 2019-02-05 | Imagilin Technology Llc | Compositions and methods for treating inflammatory related diseases or conditions using Pediococcus acidilactici probiotics |
WO2016149366A1 (en) | 2015-03-16 | 2016-09-22 | The Johns Hopkins University | Methods and compositions for treating cancer |
US10946050B2 (en) | 2015-03-16 | 2021-03-16 | Imagilin Technology Llc | Compositions comprising probiotics and methods of use thereof |
US9809625B2 (en) | 2015-03-18 | 2017-11-07 | Bristol-Myers Squibb Company | Immunomodulators |
WO2016153948A1 (en) | 2015-03-20 | 2016-09-29 | Deuterx, Llc | Combination therapy using enantiopure, oxy-substituted, deuterium-enriched 5-(benzyl)-5-deutero-thiazolidine-2, 4-diones for treatment of medical disorders |
MX2017012113A (en) | 2015-03-20 | 2018-07-06 | Syndax Pharmaceuticals Inc | Combination of hdac inhibitor and anti-pd-1 antibody for treatment of cancer. |
US20180044418A1 (en) | 2015-03-20 | 2018-02-15 | Merck Sharp & Dohme Corp. | Combination of a pd-1 antagonist and vorinostat for treating cancer |
WO2016154082A2 (en) | 2015-03-23 | 2016-09-29 | Tang Yao | Methods of primary tissue culture and drug screening using autologous serum and fluids |
CA2979712C (en) | 2015-03-25 | 2024-01-23 | The Regents Of The University Of Michigan | Nanoparticle compositions for delivery of biomacromolecules |
US10302629B2 (en) | 2015-03-30 | 2019-05-28 | University Of Maryland, Baltimore | Compositions and methods for treating cancer by rational targeting of protein translation |
KR20190057158A (en) | 2015-04-02 | 2019-05-27 | 길리애드 사이언시즈, 인코포레이티드 | Polycyclic-carbamoylpyridone compounds and their pharmaceutical use |
JP6921001B2 (en) | 2015-04-13 | 2021-08-18 | ファイザー・インク | Chimeric antigen receptor that targets B cell maturation antigens |
WO2016166600A1 (en) | 2015-04-15 | 2016-10-20 | Trojantec Technologies Ltd | Delivery of microrna using mesenchymal stem cell microparticles |
EP3283463B1 (en) | 2015-04-17 | 2021-01-20 | The Trustees Of The University Of Pennsylvania | Dimeric quinacrine derivatives as autophagy inhibitors for cancer therapy |
CN108135177B (en) | 2015-04-29 | 2021-06-01 | 雷迪厄斯制药公司 | Methods for treating cancer |
UY36660A (en) | 2015-04-30 | 2016-11-30 | Bayer Pharma AG | IRAK4 INHIBITORS COMBINATIONS |
US20180140694A1 (en) | 2015-05-04 | 2018-05-24 | Bionor Immuno As | Dosage regimen for hiv vaccine |
TN2017000467A1 (en) | 2015-05-05 | 2019-04-12 | Bayer Pharma AG | Amido-substituted cyclohexane derivatives |
US9840503B2 (en) * | 2015-05-11 | 2017-12-12 | Incyte Corporation | Heterocyclic compounds and uses thereof |
WO2016187122A1 (en) | 2015-05-15 | 2016-11-24 | University Of Iowa Research Foundation | Methods for treating tumors in situ including intratumor injection of cytotoxic particles and immune checkpoint blockade therapy |
WO2016184973A1 (en) | 2015-05-19 | 2016-11-24 | Innavirvax | Treatment of hiv-infected individuals |
US20160339030A1 (en) | 2015-05-19 | 2016-11-24 | University Of Maryland, Baltimore | Treatment agents for inhibiting hiv and cancer in hiv infected patients |
WO2016184963A1 (en) | 2015-05-19 | 2016-11-24 | Innavirvax | Treatment of hiv-infected individuals |
WO2016184962A1 (en) | 2015-05-19 | 2016-11-24 | Innavirvax | Treatment of hiv-infected individuals |
IL255769B2 (en) | 2015-05-20 | 2023-09-01 | Broad Inst Inc | Shared neoantigens |
CA2985194C (en) | 2015-05-21 | 2024-05-21 | Chemocentryx, Inc. | Ccr2 modulators |
CN107708674A (en) | 2015-05-22 | 2018-02-16 | 阿菲欧斯公司 | combination HIV therapy |
EP3303326B1 (en) | 2015-05-26 | 2020-12-16 | H. Hoffnabb-La Roche Ag | Heterocyclic estrogen receptor modulators and uses thereof |
CN104892648A (en) | 2015-05-27 | 2015-09-09 | 天津工业大学 | Preparation and application of target metal organic frameworks carrying antitumor drug |
US20180164317A1 (en) | 2015-05-28 | 2018-06-14 | Bayer Pharma Aktiengesellschaft | Method for stratification of melanoma patients by determination of oxygen consumption, ppargc1a, ppargc1b and mitf levels |
WO2016196471A1 (en) | 2015-06-02 | 2016-12-08 | Cooper Human Systems Llc | Methods and compositions for treatment of hiv infection |
WO2016197009A1 (en) | 2015-06-05 | 2016-12-08 | Vertex Pharmaceuticals Incorporated | Triazoles for the treatment of demyelinating diseases |
CA2986949C (en) | 2015-06-05 | 2020-07-21 | MiRagen Therapeutics, Inc. | Mir-155 inhibitors for treating cutaneous t cell lymphoma (ctcl) |
US10370339B2 (en) | 2015-06-08 | 2019-08-06 | Bayer Pharma Aktiengesellschaft | N-Methylbenzimidazoles as mIDH1 inhibitors |
US10702527B2 (en) | 2015-06-12 | 2020-07-07 | Dana-Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
WO2015151078A2 (en) | 2015-06-15 | 2015-10-08 | Suzhou M-Conj Biotech Co., Ltd | Hydrophilic linkers for conjugation |
WO2016205566A1 (en) | 2015-06-16 | 2016-12-22 | The Regents Of The University Of California | Fzd7 specific antibodies and vaccines to treat cancer and control stem cell function |
US10975112B2 (en) | 2015-06-16 | 2021-04-13 | Hangzhou Dac Biotech Co., Ltd. | Linkers for conjugation of cell-binding molecules |
US10766962B2 (en) | 2015-06-16 | 2020-09-08 | The Regents Of The University Of California | FZD7 specific antibodies and vaccines to treat cancer and control stem cell function |
WO2016202756A1 (en) | 2015-06-18 | 2016-12-22 | Bayer Pharma Aktiengesellschaft | Substituted 2-(1h-pyrazol-1-yl)-1h-benzimidazole compounds |
WO2016202758A1 (en) | 2015-06-18 | 2016-12-22 | Bayer Pharma Aktiengesellschaft | Substituted 2-(1h-pyrazol-1-yl)-1h-benzimidazole compounds |
CN116712552A (en) | 2015-06-19 | 2023-09-08 | 波士顿大学托管委员会 | Methods and compositions for treating herpes virus-induced conditions |
CN107921144B (en) | 2015-06-20 | 2023-11-28 | 杭州多禧生物科技有限公司 | Aureostatin analogs and conjugate conjugates thereof with cell-binding molecules |
MX2017017172A (en) | 2015-06-22 | 2018-02-23 | Bayer Pharma AG | BINDING-ACTIVE PRINCIPLE CONJUGATES (ADCS) AND BINDING-PROFARMACO CONJUGATES (APDCS) WITH ENZYMATICALLY SCINDIBLE GROUPS. |
EP3313521A1 (en) | 2015-06-23 | 2018-05-02 | Bayer Pharma Aktiengesellschaft | Antibody drug conjugates of kinesin spindel protein (ksp) inhibitors with anti-tweakr-antibodies |
CA2990300A1 (en) | 2015-06-23 | 2016-12-29 | Hans-Georg Lerchen | Site specific homogeneous conjugates with ksp inhibitors |
US10744205B2 (en) | 2015-06-23 | 2020-08-18 | Bayer Pharma Aktiengesellschaft | Antibody drug conjugates of kinesin spindel protein (KSP) inhibitors with anti-CD123-antibodies |
WO2016210247A1 (en) | 2015-06-24 | 2016-12-29 | Duke University | New methods of use for an anti-diarrhea agent |
EP3313388A4 (en) | 2015-06-24 | 2019-05-15 | Duke University | CHEMICAL MODULATORS OF SIGNALING PATHWAYS AND THERAPEUTIC USE |
KR20240090657A (en) | 2015-06-29 | 2024-06-21 | 아브락시스 바이오사이언스, 엘엘씨 | Methods of treating solid tumors using nanoparticle mtor inhibitor combination therapy |
CA2985859A1 (en) | 2015-06-29 | 2017-01-05 | Merck Patent Gmbh | Tbk/ikk.epsilon. inhibitor compounds and uses thereof |
AU2016285597A1 (en) | 2015-06-29 | 2018-01-18 | Syndax Pharmaceuticals, Inc. | Combination of HDAC inhibitor and anti-PD-L1 antibody for treatment of cancer |
CN107921050A (en) | 2015-06-29 | 2018-04-17 | 阿布拉科斯生物科学有限公司 | Use the method for nano particle MTOR inhibitor conjoint therapy treatment haematological malignancies |
UY36758A (en) | 2015-06-30 | 2016-12-30 | Glaxosmithkline Ip No 2 Ltd | INHIBITORS OF THE ZESTE 2 HOMOLOGIST POTENTIATOR |
US10925852B2 (en) | 2015-06-30 | 2021-02-23 | The Trustees Of Columbia University In The City Of New York | Talc-bound compositions and uses thereof |
CA2991384C (en) | 2015-07-04 | 2022-11-08 | Suzhou M-Conj Biotech Co., Ltd | Bridge linkers for conjugation of a cell-binding molecule |
US10179123B2 (en) | 2015-07-07 | 2019-01-15 | Bayer Pharma Aktiengesellschaft | 2-aryl- and 2-arylalkyl-benzimidazoles as mIDH1 inhibitors |
WO2017008046A1 (en) | 2015-07-08 | 2017-01-12 | Children's Hospital Medical Center | Loss of transcriptional fidelity leads to immunotherapy resistance in cancers |
US10045985B2 (en) | 2015-07-09 | 2018-08-14 | Merck Patent Gmbh | Heteroaryl compounds as BTK inhibitors and uses thereof |
WO2017005711A1 (en) | 2015-07-09 | 2017-01-12 | Bayer Pharma Aktiengesellschaft | Phosphorous-and sulfur-substituted benzodiazepine derivatives |
US9839687B2 (en) | 2015-07-15 | 2017-12-12 | Suzhou M-Conj Biotech Co., Ltd. | Acetylenedicarboxyl linkers and their uses in specific conjugation of a cell-binding molecule |
US10292961B2 (en) | 2015-07-15 | 2019-05-21 | Hangzhou Dac Biotech Co., Ltd. | Disulfur bridge linkers for conjugation of a cell-binding molecule |
US10414734B2 (en) | 2015-07-16 | 2019-09-17 | Bayer Pharma Aktiengesellschaft | 5-hydroxyalkylbenzimidazoles as mIDH1 inhibitors |
EP3121166A1 (en) | 2015-07-21 | 2017-01-25 | Bayer Pharma Aktiengesellschaft | Fused imidazoles as midh1 inhibitors |
GB201512869D0 (en) | 2015-07-21 | 2015-09-02 | Almac Diagnostics Ltd | Gene signature for minute therapies |
WO2017019767A1 (en) | 2015-07-27 | 2017-02-02 | Myosotis, Llc | Inhibition of CXCL12 in Cancer Immunotherapy |
CA2993644A1 (en) | 2015-07-28 | 2017-02-02 | Beta Cat Pharmaceuticals, Inc. | Anthracene-9, 10-dione dioxime compounds prodrugs and their uses |
ES2878188T3 (en) | 2015-07-29 | 2021-11-18 | Novartis Ag | Combination therapies comprising antibody molecules against LAG-3 |
US20180207273A1 (en) | 2015-07-29 | 2018-07-26 | Novartis Ag | Combination therapies comprising antibody molecules to tim-3 |
CN108025051B (en) | 2015-07-29 | 2021-12-24 | 诺华股份有限公司 | Combination therapy comprising anti-PD-1 antibody molecules |
EP3124609A1 (en) | 2015-07-29 | 2017-02-01 | IFOM Fondazione Istituto Firc di Oncologia Molecolare | Therapeutics oligonucleotides |
WO2017018476A1 (en) | 2015-07-29 | 2017-02-02 | 塩野義製薬株式会社 | Salt of quinazoline derivative or crystal thereof, and method for producing salt of quinazoline derivative or crystal thereof |
CA2993796C (en) | 2015-07-29 | 2024-02-20 | Onkimmune Limited | Modified natural killer cells and natural killer cell lines having increased cytotoxicity |
EP3735977A1 (en) | 2015-07-31 | 2020-11-11 | Vascular Biogenics Ltd. | Motile sperm domain containing protein 2 and cancer |
WO2017024009A1 (en) | 2015-08-03 | 2017-02-09 | Quadriga Biosciences, Inc. | Beta-substituted beta-amino acids and analogs as chemotherapeutic agents and uses thereof |
WO2017021348A1 (en) | 2015-08-05 | 2017-02-09 | Bayer Pharma Aktiengesellschaft | 1h-pyrrol-3-amines |
WO2017023994A1 (en) | 2015-08-06 | 2017-02-09 | Yale University | Small molecule based antibody-recruiting compounds for cancer treatment |
CA2993624A1 (en) | 2015-08-07 | 2017-02-16 | Thomas Helledays Stiftelse For Medicinsk Forskning | Method for diagnosisng cancer or cancer-associated thrombosis by measuring levels of h3cit in plasma |
US10363226B2 (en) | 2015-08-12 | 2019-07-30 | North Carolina State University | Platelet membrane-coated drug delivery system |
WO2017025493A1 (en) | 2015-08-12 | 2017-02-16 | Bayer Pharma Aktiengesellschaft | Quinoline ezh2 inhibitors |
WO2017031041A1 (en) | 2015-08-17 | 2017-02-23 | Channel Therapeutics, Inc. | Functionalized aminobenzoboroxoles |
EP3133165A1 (en) | 2015-08-17 | 2017-02-22 | F. Hoffmann-La Roche AG | Methods for personalizing patient cancer therapy with anti angiogenic compounds |
GB201514756D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compound and method of use |
WO2017034234A1 (en) | 2015-08-21 | 2017-03-02 | 서울대학교 산학협력단 | Composite formulation for treating cancer having hdac inhibitor resistance |
US20170056352A1 (en) | 2015-08-25 | 2017-03-02 | Rgenix, Inc. | PHARMACEUTICALLY ACCEPTABLE SALTS OF beta-GUANIDINOPROPIONIC ACID WITH IMPROVED PROPERTIES AND USES THEREOF |
US20180250320A1 (en) | 2015-08-26 | 2018-09-06 | The Johns Hopkins University | Compositions and methods for treating solid tumors |
US20210292327A1 (en) | 2015-08-26 | 2021-09-23 | Gilead Sciences, Inc. | Deuterated toll-like receptor modulators |
US11096934B2 (en) | 2015-09-01 | 2021-08-24 | The Broad Institute, Inc. | Compounds and methods useful for treating or preventing hematological cancers |
RU2018111407A (en) | 2015-09-02 | 2019-10-03 | Синдакс Фармасьютикалз, Инк. | SELECTION OF PATIENTS FOR COMBINED THERAPY |
US10588985B2 (en) | 2015-09-02 | 2020-03-17 | Wayne State University | Compositions and methods relating to RAD6 inhibition |
JP6971970B2 (en) | 2015-09-03 | 2021-11-24 | エルロン・セラピューティクス・インコーポレイテッドAileron Therapeutics, Inc. | Peptidomimetic macrocyclic molecules and their use |
DE102015012050A1 (en) | 2015-09-15 | 2017-03-16 | Merck Patent Gmbh | Compounds as ASIC inhibitors and their uses |
DE102015012049A1 (en) | 2015-09-15 | 2017-03-16 | Merck Patent Gmbh | Compounds as ASIC inhibitors and their uses |
ES2980858T3 (en) | 2015-09-15 | 2024-10-03 | Stichting Radboud Univ Medisch Centrum | Improved method for ex vivo expansion of CD34+ HSPCs into NK cells using an aryl hydrocarbon receptor antagonist |
MX2018002986A (en) | 2015-09-18 | 2018-05-02 | Merck Patent Gmbh | Heteroaryl compounds as irak inhibitors and uses thereof. |
EP3350177B1 (en) | 2015-09-18 | 2021-07-07 | Merck Patent GmbH | Heteroaryl compounds as irak inhibitors and uses thereof |
US20210393674A1 (en) | 2015-09-20 | 2021-12-23 | Air Cross, Inc. | Ozonolysis for activation of compounds and degradation of ozone |
RU2018114459A (en) | 2015-09-21 | 2019-10-23 | Ифом Фондационе Иституто Фирк Ди Онколоджа Молеколаре | NEW BLOOD CANCER TREATMENT STRATEGIES |
MX377124B (en) | 2015-09-21 | 2025-03-07 | Plexxikon Inc | HETEROCYCLIC COMPOUNDS AND THEIR USES. |
WO2017053823A1 (en) | 2015-09-25 | 2017-03-30 | Pharmacyclics Llc | Treatment using hdac inhibitors and immunotherapy |
US20180271849A1 (en) | 2015-09-29 | 2018-09-27 | Kangpu Biopharmaceuticals, Ltd. | Pharmaceutical composition and application thereof |
CA2999516A1 (en) | 2015-09-30 | 2017-04-06 | Gilead Sciences, Inc. | Compounds and combinations for the treatment of hiv |
WO2017055313A1 (en) | 2015-10-01 | 2017-04-06 | Bayer Pharma Aktiengesellschaft | Amido-substituted azole compounds |
ES2900482T3 (en) | 2015-10-01 | 2022-03-17 | Gilead Sciences Inc | Combination of a Btk inhibitor and a checkpoint inhibitor for cancer treatment |
WO2017055316A1 (en) | 2015-10-01 | 2017-04-06 | Bayer Pharma Aktiengesellschaft | Amido-substituted azole compounds |
EP3355888B8 (en) | 2015-10-02 | 2022-04-13 | Pierre Fabre Medicament | Hemi-synthetic trilobine analogs for use as a drug |
WO2017059252A1 (en) | 2015-10-02 | 2017-04-06 | Gilead Sciences, Inc. | Combinations of the btk inhibitor gs-4059 with inhibitors selected from a jak, ask1, brd and/or mmp9 inhibitor to treat cancer, allergic disorders, autoimmune diseases or inflammatory diseases |
HUE054985T2 (en) | 2015-10-09 | 2021-11-29 | Boehringer Ingelheim Int | Spiro [3H-indole-3,2'-pyrrolidin] -2 (1H) -one compounds and numbers as MDM2-P53 inhibitors |
WO2017060322A2 (en) | 2015-10-10 | 2017-04-13 | Bayer Pharma Aktiengesellschaft | Ptefb-inhibitor-adc |
WO2017063966A1 (en) | 2015-10-13 | 2017-04-20 | Bayer Pharma Aktiengesellschaft | Substituted 2-(1h-pyrazol-1-yl)-benzothiazole compounds |
CN105288648B (en) | 2015-10-14 | 2018-11-06 | 东南大学 | A kind of phosphatide cpd of hydrophilic medicament, its pharmaceutical composition and application |
US20180346877A1 (en) | 2015-10-15 | 2018-12-06 | Celularity, Inc. | Natural killer cells and ilc3 cells and uses thereof |
WO2017063959A1 (en) | 2015-10-15 | 2017-04-20 | Bayer Pharma Aktiengesellschaft | N-sulphoximinophenyl-substituted benzodiazepine derivatives as bet protein inhibitors |
US20190055563A1 (en) | 2015-10-19 | 2019-02-21 | Dana-Farber Cancer Institute, Inc. | Polymerase q as a target in hr-deficient cancers |
KR20180067677A (en) | 2015-10-23 | 2018-06-20 | 다이이찌 산쿄 가부시키가이샤 | Pharmaceutical compositions for use in the treatment of AML and methods of treating AML in subjects in need thereof |
US20170115275A1 (en) | 2015-10-23 | 2017-04-27 | Arizona Board Of Regents On Behalf Of Arizona State University | Engineered substrates for high-throughput generation of 3d models of tumor dormancy, relapse and micrometastases for phenotype specific drug discovery and development |
JP6855472B2 (en) | 2015-10-23 | 2021-04-07 | 第一三共株式会社 | MDM2 inhibitor dosing regimen to treat cancer |
WO2017074788A1 (en) | 2015-10-27 | 2017-05-04 | The Broad Institute Inc. | Compositions and methods for targeting cancer-specific sequence variations |
WO2017075451A1 (en) | 2015-10-28 | 2017-05-04 | The Broad Institute Inc. | Compositions and methods for evaluating and modulating immune responses by detecting and targeting pou2af1 |
WO2017075478A2 (en) | 2015-10-28 | 2017-05-04 | The Broad Institute Inc. | Compositions and methods for evaluating and modulating immune responses by use of immune cell gene signatures |
WO2017075465A1 (en) | 2015-10-28 | 2017-05-04 | The Broad Institute Inc. | Compositions and methods for evaluating and modulating immune responses by detecting and targeting gata3 |
LT3370768T (en) | 2015-11-03 | 2022-05-25 | Janssen Biotech, Inc. | Antibodies specifically binding pd-1 and their uses |
US20190038713A1 (en) | 2015-11-07 | 2019-02-07 | Multivir Inc. | Compositions comprising tumor suppressor gene therapy and immune checkpoint blockade for the treatment of cancer |
CN105457038A (en) | 2015-11-09 | 2016-04-06 | 东南大学 | Quick release type medicine phosphatide compound and medicine composition thereof |
MX2018005830A (en) | 2015-11-10 | 2018-11-12 | Univ Yale | Compositions and methods for treating autoimmune diseases and cancers. |
AU2016352572B2 (en) | 2015-11-12 | 2023-10-19 | Hookipa Biotech Gmbh | Arenavirus particles as cancer vaccines |
WO2017086367A1 (en) | 2015-11-18 | 2017-05-26 | 中外製薬株式会社 | Combination therapy using t cell redirection antigen binding molecule against cell having immunosuppressing function |
TWI724056B (en) | 2015-11-19 | 2021-04-11 | 美商卡默森屈有限公司 | Inhibitors of cxcr2 |
TWI734715B (en) | 2015-11-19 | 2021-08-01 | 美商卡默森屈有限公司 | Modulators of chemokine receptors |
AU2016355268B2 (en) | 2015-11-20 | 2021-08-19 | Senhwa Biosciences, Inc. | Combination therapy of tetracyclic quinolone analogs for treating cancer |
EP3440579A4 (en) | 2015-11-24 | 2020-03-25 | Klaritos, Inc. | Novel healthcare delivery, treatment, and payment model for specialty drugs |
UA126897C2 (en) | 2015-12-01 | 2023-02-22 | Генмаб Б.В. | ANTIBODIES AGAINST DR5 AND METHODS OF THEIR APPLICATION |
WO2017091865A1 (en) | 2015-12-03 | 2017-06-08 | Alfred Health | Monitoring treatment or progression of myeloma |
US10654818B2 (en) | 2015-12-03 | 2020-05-19 | Bayer Pharma Aktiengesellschaft | Furane derivatives as inhibitors of ATAD2 |
US10722529B2 (en) | 2015-12-03 | 2020-07-28 | Temple University—Of the Commonwealth System of Higher Education | Modulation of NAD+ metabolic pathways for treatment of disease |
PH12018501155B1 (en) | 2015-12-04 | 2024-06-28 | Boehringer Ingelheim Int | Biparatopic polypeptides antagonizing wnt signaling in tumor cells |
CN106821965A (en) | 2015-12-04 | 2017-06-13 | 中国科学院大连化学物理研究所 | A kind of vitamin A acid multiple medicine delivers nanoparticle solution and its preparation and application altogether |
CN108368143B (en) | 2015-12-09 | 2022-02-01 | 维也纳医科大学 | Monomaleimide functionalized platinum compounds for cancer therapy |
US10969392B2 (en) | 2015-12-10 | 2021-04-06 | Vanderbilt University | Methods and systems for predicting response to immunotherapies for treatment of cancer |
TWI814056B (en) | 2015-12-15 | 2023-09-01 | 美商基利科學股份有限公司 | Human immunodeficiency virus neutralizing antibodies |
US20200216439A1 (en) | 2015-12-16 | 2020-07-09 | Bayer Pharma Aktiengesellschaft | Hetero-1,5,6,7-tetrahydro-4h-indol-4-ones |
CN109069570A (en) | 2015-12-16 | 2018-12-21 | 默沙东公司 | Anti- LAG3 antibody and antigen-binding fragment |
JP6882299B2 (en) | 2015-12-17 | 2021-06-02 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | Polycyclic TLR7 / 8 antagonists and their use in the treatment of immune disorders |
CA3006772A1 (en) | 2015-12-17 | 2017-06-22 | Gilead Sciences, Inc. | Tank-binding kinase inhibitor compounds |
US20180371093A1 (en) | 2015-12-17 | 2018-12-27 | Novartis Ag | Antibody molecules to pd-1 and uses thereof |
EP3389711A1 (en) | 2015-12-18 | 2018-10-24 | Novartis AG | Antibodies targeting cd32b and methods of use thereof |
WO2017102091A1 (en) | 2015-12-18 | 2017-06-22 | Bayer Pharma Aktiengesellschaft | Heteroarylbenzimidazole compounds |
US20200268720A1 (en) | 2015-12-22 | 2020-08-27 | Glaxosmithkline Llc | Methods of use of a class iia hdac inhibitor |
EP3405587A4 (en) | 2015-12-23 | 2019-10-30 | Moonshot Pharma LLC | METHODS OF INDUCING AN IMMUNE RESPONSE BY ENABLING READING OF PREMATURE STOP CODONS |
WO2017117196A1 (en) | 2015-12-28 | 2017-07-06 | Syndax Pharmaceuticals, Inc. | Combination of hdac inhibitor and anti-pd-l1 antibody for treatment of ovarian cancer |
US10189797B2 (en) | 2015-12-30 | 2019-01-29 | Duke University | Chemical modulators of immune checkpoints and therapeutic use |
ES2964746T3 (en) | 2015-12-30 | 2024-04-09 | Celgene Corp | Methods of production of T lymphocytes and T lymphocytes produced by the same |
US20190183870A1 (en) | 2016-01-05 | 2019-06-20 | The United States Of America, As Represented By The Secretary, Dept. Of Health And Human Services | Combination of histone deacetylase inhibitor and immunotherapy |
DK3400291T4 (en) | 2016-01-08 | 2024-04-02 | Replimune Ltd | Engineered virus |
AU2017207291B2 (en) | 2016-01-11 | 2023-06-15 | The Rockefeller University | Methods for the treatment of myeloid derived suppressor cells related disorders |
WO2017121684A1 (en) | 2016-01-14 | 2017-07-20 | Bayer Pharma Aktiengesellschaft | 5-substituted 2-(morpholin-4-yl)-1,7-naphthyridines |
WO2017127414A1 (en) | 2016-01-19 | 2017-07-27 | Celgene Corporation | Transgenic mouse expressing human cereblon |
EP3405177A1 (en) | 2016-01-19 | 2018-11-28 | Janssen Pharmaceutica NV | Formulations/compositions comprising a btk inhibitor |
US10973843B2 (en) | 2016-01-27 | 2021-04-13 | University Of Maryland, Baltimore | Method for monitoring cancer and for regulation of semaphorin 4D to improve cancer immunotherapy regimens |
RU2018130831A (en) | 2016-01-28 | 2020-03-02 | Индиана Юниверсити Рисерч Энд Текнолоджи Корпорейшн | APPLICATION OF HISTONIC DEACETHYLASE INHIBITORS TO IMPROVE IMMUNOTHERAPY |
DK3408407T3 (en) | 2016-01-29 | 2021-02-08 | Epigenomics Ag | METHODS FOR DETECTING CPG METHYLATION OF TUMOR-DERIVATED DNA IN BLOOD SAMPLES |
TN2018000271A1 (en) | 2016-02-01 | 2020-01-16 | Bayer Pharma AG | Copanlisib biomarkers. |
GB201601773D0 (en) | 2016-02-01 | 2016-03-16 | Renishaw Plc | Method |
AU2017215096A1 (en) | 2016-02-01 | 2018-08-09 | Bayer Pharma Aktiengesellschaft | Copanlisib biomarkers |
WO2017134116A1 (en) | 2016-02-02 | 2017-08-10 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and pharmaceutical compositions for enhancing cd8+ t cell-dependent immune responses in subjects suffering from cancer |
WO2017136342A1 (en) | 2016-02-02 | 2017-08-10 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Fulvestrant for inducing immune-mediated cytotoxic lysis of cancer cells |
MY195114A (en) | 2016-02-04 | 2023-01-10 | Robert Yongxin Zhao | Specific Conjugation Linkers, Specific Immunoconjugates Thereof, Methods of Making and uses Such Conjugates Thereof |
CA3013402C (en) | 2016-02-05 | 2024-05-28 | Bayer Pharma Aktiengesellschaft | Compounds, compositions and methods for cancer patient stratification and cancer treatment |
US10912748B2 (en) | 2016-02-08 | 2021-02-09 | Beyondspring Pharmaceuticals, Inc. | Compositions containing tucaresol or its analogs |
CN108601841A (en) | 2016-02-10 | 2018-09-28 | 免疫医疗公司 | The combination of ABCG2 inhibitor and SACITUZUMAB GOVITECAN (IMMU-132) overcome the resistance to SN-38 in the cancer for expressing TROP-2 |
WO2017143035A2 (en) | 2016-02-17 | 2017-08-24 | The Penn State Research Foundation | Method and therapeutic use of pign and other genes or genes products that pign interacts with for prognosis and treatment of hematological neoplasias |
WO2017143237A1 (en) | 2016-02-17 | 2017-08-24 | Acetylon Pharmaceuticals, Inc. | Increasing expression of interferon regulated genes with combinatons of histone deacetylase inhibitors and immunomodulatory drugs |
US20200121699A1 (en) | 2016-02-22 | 2020-04-23 | Onxeo | Combination therapies comprising immuno-oncology agents and belinostat |
JP2019511919A (en) | 2016-02-23 | 2019-05-09 | ブローディ,チャヤ | Production of cancer stem cells and use thereof |
US20170247690A1 (en) | 2016-02-25 | 2017-08-31 | Agenovir Corporation | Oncoviral treatment with nuclease and chemotherapeutic |
AU2017228371A1 (en) | 2016-03-04 | 2018-09-13 | Gilead Sciences, Inc. | Compositions and combinations of autotaxin inhibitors |
US10143746B2 (en) | 2016-03-04 | 2018-12-04 | Bristol-Myers Squibb Company | Immunomodulators |
WO2017148995A1 (en) | 2016-03-04 | 2017-09-08 | Bayer Pharma Aktiengesellschaft | 1-(pyrimidin-2-yl)-1h-indazoles having bub1 kinase inhibiting activity |
CN109071669A (en) | 2016-03-07 | 2018-12-21 | 查尔斯顿制药有限责任公司 | Anti- paranuclein antibody |
EP3426657B1 (en) | 2016-03-08 | 2022-07-13 | Bayer Pharma Aktiengesellschaft | 2 amino n [7 methoxy 2, 3-dihydroimidazo-[1, 2-c]quinazolin-5-yl]pyrimidine 5 carboxamides |
WO2017156147A1 (en) | 2016-03-08 | 2017-09-14 | The Board Of Regents For Oklahoma State University Office Of Intellectual Property Management Technology Development Center | Immune boosting dietary compounds for disease control and prevention |
US10717774B2 (en) | 2016-03-14 | 2020-07-21 | Kiromic, Inc. | Compositions and methods for treating cancers |
WO2017160717A2 (en) | 2016-03-15 | 2017-09-21 | Memorial Sloan Kettering Cancer Center | Method of treating diseases using kinase modulators |
WO2017157418A1 (en) | 2016-03-15 | 2017-09-21 | Bayer Pharma Aktiengesellschaft | Combination of mknk1-inhibitors |
US20170268001A1 (en) | 2016-03-16 | 2017-09-21 | The University Of Chicago | Rnas with tumor radio/chemo-sensitizing and immunomodulatory properties and methods of their preparation and application |
EP3219329A1 (en) | 2016-03-17 | 2017-09-20 | Bayer Pharma Aktiengesellschaft | Combinations of copanlisib |
WO2017157991A1 (en) | 2016-03-18 | 2017-09-21 | Bayer Pharma Aktiengesellschaft | 1-alkyl-pyrazoles and -indazoles as bub1 inhibitors for the treatment of hyperproliferative diseases |
WO2017157992A1 (en) | 2016-03-18 | 2017-09-21 | Bayer Pharma Aktiengesellschaft | Annulated pyrazoles as bub1 kinase inhibitors for treating proliferative disorders |
WO2017161331A1 (en) | 2016-03-18 | 2017-09-21 | Procept Biorobotics Corporation | Minimally invasive methods and systems for hemostasis in a bleeding closed tissue volume |
US20170273926A1 (en) | 2016-03-24 | 2017-09-28 | Orbus Therapeutics, Inc. | Compositions and methods for use of eflornithine and derivatives and analogs thereof to treat cancers, including gliomas |
TWI808055B (en) | 2016-05-11 | 2023-07-11 | 美商滬亞生物國際有限公司 | Combination therapies of hdac inhibitors and pd-1 inhibitors |
TWI794171B (en) | 2016-05-11 | 2023-03-01 | 美商滬亞生物國際有限公司 | Combination therapies of hdac inhibitors and pd-l1 inhibitors |
CN105949114A (en) | 2016-06-27 | 2016-09-21 | 山东川成医药股份有限公司 | Synthesis method of chidamide |
EP3487492A4 (en) | 2016-07-20 | 2020-03-11 | Eisai R&D Management Co., Ltd. | Use of eribulin and histone deacetylase inhibitors in the treatment of cancer |
CN106866571B (en) | 2017-01-20 | 2018-06-29 | 中国药科大学 | Heterocyclic urea compound and its pharmaceutical composition and application |
RU2733950C1 (en) | 2017-02-13 | 2020-10-08 | Канпу Биофармасьютикалс, Лтд. | Combination for treating prostate cancer, a pharmaceutical composition and a method of treating |
CN106916101B (en) | 2017-02-15 | 2020-05-01 | 聚缘(上海)生物科技有限公司 | NAMPT/HDAC dual-target inhibitor and preparation method thereof |
CN107011238B (en) | 2017-03-14 | 2020-05-01 | 北京化工大学 | Histone deacetylase inhibitor and preparation method and application thereof |
JP7187486B2 (en) | 2017-05-25 | 2022-12-12 | レイドス, インコーポレイテッド | PD-1 and CTLA-4 Dual Inhibitor Peptides |
US20190046513A1 (en) | 2017-08-10 | 2019-02-14 | Huya Bioscience International, Llc | Combination therapies of hdac inhibitors and tubulin inhibitors |
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Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015157162A1 (en) * | 2014-04-06 | 2015-10-15 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Histone deacetylase as a modulator of pdl1 expression and activity |
Non-Patent Citations (4)
Title |
---|
ANONYMOUS: "Study of HBI-8000 With Nivolumab in Melanoma, Renal Cell Carcinoma and Non-Small Cell Lung Cancer - NCT02718066", CLINICALTRIALS.GOV, 24 March 2016 (2016-03-24), Internet, pages 1 - 9, XP055647346, Retrieved from the Internet <URL:https://clinicaltrials.gov/ct2/show/record/NCT02718066> [retrieved on 20191128] * |
DAVID M WOODS ET AL: "Abstract 257: Class I HDAC inhibition upregulates PD-1 ligands in melanoma and increases the efficacy of PD-1 blockade", PROCEEDINGS: AACR 106TH ANNUAL MEETING, 18 April 2015 (2015-04-18), pages 1 - 2, XP055647334, Retrieved from the Internet <URL:https://cancerres.aacrjournals.org/content/75/15_Supplement/257> [retrieved on 20191128], DOI: 10.1158/1538-7445.AM2015-257 * |
REID P BISSONNETTE ET AL: "Abstract B108: The HDAC inhibitor HBI-8000 enhances immunotherapy with either PD-1 or PD-L1 blockade in the MC38 model of colon cancer", vol. 4, no. 11 Suppl, 25 September 2016 (2016-09-25), XP002795767, Retrieved from the Internet <URL:https://cancerimmunolres.aacrjournals.org/content/4/11_Supplement/B108> [retrieved on 20191031], DOI: 10.1158/2326-6066.IMM2016-B108 * |
ZHI-QIANG NING ET AL: "Chidamide (CS055/HBI-8000): a new histone deacetylase inhibitor of the benzamide class with antitumor activity and the ability to enhance immune cell-mediated tumor cell cytotoxicity", CANCER CHEMOTHERAPY AND PHARMACOLOGY, SPRINGER, BERLIN, DE, vol. 69, no. 4, 12 November 2011 (2011-11-12), pages 901 - 909, XP035035155, ISSN: 1432-0843, DOI: 10.1007/S00280-011-1766-X * |
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